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Concentrating on molecular biomarkers in cancer research, Cancer Biomarkers publishes original research findings (and reviews solicited by the editor) on the subject of the identification of markers associated with the disease processes whether or not they are an integral part of the pathological lesion.
The disease markers may include, but are not limited to, genomic, epigenomic, proteomics, cellular and morphologic, and genetic factors predisposing to the disease or indicating the occurrence of the disease. Manuscripts on these factors or biomarkers, either in altered forms, abnormal concentrations or with abnormal tissue distribution leading to disease causation will be accepted.
Authors: Latini, Giuseppe | De Felice, Claudio | Barducci, Alessandro | Dipaola, Lucia | Gentile, Mattia | Andreassi, Maria Grazia | Correale, Mario | Bianciardi, Giorgio
Article Type: Research Article
Abstract: Cancer is the most important cause of death worldwide, and early cancer detection is the most fundamental factor for efficacy of treatment, prognosis, and increasing survival rate. Over the years great effort has been devoted to discovering and testing new biomarkers that can improve its diagnosis, especially at an early stage. Here we report the potential usefulness of new, easily applicable, non-invasive and relatively low-cost clinical biomarkers, based on abnormalities of oral mucosa spectral reflectance and fractal geometry of the vascular networks in several different tissues, for identification of hereditary non-polyposis colorectal cancer carriers as well for detection of other …tumors, even at an early stage. In the near future the methodology/technology of these procedures should be improved, thus making possible their applicability worldwide as screening tools for early recognition and prevention of cancer. Show more
Keywords: Clinical biomarkers, cancer, oral mucosal network abnormalities, fractal analysis, oral mucosal spectral reflectance
DOI: 10.3233/CBM-170050
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 179-198, 2018
Authors: Fricke, A. | Cimniak, A.F.V. | Ullrich, P.V. | Becherer, C. | Bickert, C. | Pfeifer, D. | Heinz, J. | Stark, G.B. | Bannasch, H. | Braig, D. | Eisenhardt, S.U.
Article Type: Research Article
Abstract: BACKGROUND: Liposarcoma constitute about 13% of all soft tissue sarcoma and are associated with a high risk of metastases. As the preoperative differentiation between benign and malign lipomatous tumors is restricted to magnetic resonance imaging, computed tomography and biopsy, we performed a miRNA array to distinguish dedifferentiated liposarcoma patients from healthy controls and lipoma patients. METHODS: Blood samples of patients with dedifferentiated liposarcoma, healthy controls and lipoma patients were collected. Whole blood RNA was extracted and samples of patients with dedifferentiated liposarcoma (n = 6) and of healthy donors (n = …4) were analyzed using an Affymetrix GeneChip miRNA Array v. 4.0. qRT-PCR was carried out to confirm the most differentially expressed miRNA; being further analyzed in an independent cohort of healthy controls as well as in lipoma patients. RESULTS: As shown by the microarray, two miRNAs (miR-3613-3p, miR-4668-5p) were shown to be significantly upregulated (fold change: > 2.5; p < 0.05) in patients with dedifferentiated liposarcoma (n = 6) as compared to healthy controls (n = 4). miR-3613-3p was further validated by qRT-PCR to be significantly upregulated in dedifferentiated liposarcoma patients compared to an independent cohort of healthy controls (n = 3) and lipoma patients (n = 5). CONCLUSION: We identified a specific whole blood miRNA (miR-3613-3p) that may serve to distinguish between dedifferentiated liposarcoma patients and healthy controls, thus potentially serving as a specific biomarker for dedifferentiated liposarcoma. Show more
Keywords: Whole-blood-RNA, miRNA, dedifferentiated liposarcoma, biomarker, liquid biopsy
DOI: 10.3233/CBM-170496
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 199-207, 2018
Authors: Tian, Chunmei | Zhang, Lin | Li, Xiaohua | Zhang, Yanjun | Li, Jianchang | Chen, Liang
Article Type: Research Article
Abstract: BACKGROUND: Abnormal expression of miR-192 has been observed in a variety of human cancers, but the expression pattern of miR-192 and its prognostic value in pediatric acute myeloid leukemia (AML) is poorly known. OBJECTIVE: This study was to explore the expression status of miR-192 and its clinical significance in pediatric patients with AML. METHODS: Quantitative RT-PCR was carried out to detect miR-192 expression level in the serum from 97 AML cases and 50 healthy controls. RESULTS: The results showed that downregulation of serum miR-192 was observed in pediatric AML patients and …strongly correlated with aggressive clinical features. Increased serum miR-192 expression occurred more frequently in the AML subjects with favorable risk cytogenetics. Moreover, serum miR-192 expression showed good performance to screen pediatric AML subjects from normal controls. Furthermore, serum miR-192 was identified as a independent prognostic indicator for both overall survival and event free survival. In addition, low serum miR-192 expression significantly contributed to poor prognosis in the whole cohort of AML patients or the AML patients with intermediate-risk cytogenetics. CONCLUSIONS: Collectively, serum miR-192 potentially can be a reliable biomarker for the diagnosis and prognosis in pediatric AML. Show more
Keywords: Acute myeloid leukemia, MiR-192, pediatric, prognosis
DOI: 10.3233/CBM-170657
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 209-215, 2018
Authors: Ding, Shimei | Qu, Wei | Jiao, Yang | Zhang, Jing | Zhang, Chunhong | Dang, Shuangsuo
Article Type: Research Article
Abstract: OBJECTIVE: To investigate the expression and role of long non-coding RNA (lncRNA) small nucleolar RNA host gene 12 (SNHG12) in papillary thyroid carcinoma (PTC). METHODS: The relative expression levels of lncRNA SNHG12 (hereinafter referred to as SNHG12) in 42 pairs of PTC tissues and para-carcinoma tissues were detected via quantitative reverse transcription polymerase chain reaction (qRT-PCR). SNHG12 specific interference sequences were designed and synthesized. The relative expression level and transfection efficiency of SNHG12 in PTC cells were detected via qRT-PCR. After the interference in SNHG12 expression, the change in cell proliferation capacity was detected via methyl …thiazolyl tetrazolium (MTT) assay, the change in cell cycle distribution was detected via flow cytometry, the changes in cell migration and invasion capacities were detected via Transwell assay and wound healing assay, and the changes in expressions of molecular markers of Wnt/β -catenin pathway were detected via Western blotting. The pulmonary metastasis model of nude mice was established, and the changes in migration and invasion capacities of tumor cells were studied via the in-vivo experiment after the interference in SNHG12 expression. RESULTS: The results of qRT-PCR showed that the SNHG12 expression was up-regulated in 30 pairs of PTC tissues and cells. The results of MTT assay showed that the cell proliferation capacity was inhibited after the interference in SNHG12. The results of flow cytometry showed that the cell cycle progression was blocked in G1-G0 phase after the knockdown of SNHG12 expression. The results of Transwell assay and Western blotting showed that the interference in SNHG12 could inhibit the invasion and metastasis capacities of tumor cells through influencing the Wnt/β -catenin signaling pathway. Metastatic tumor model of nude mice showed that SNHG12 could affect the invasion and metastasis of tumor cells in vivo . CONCLUSION: The SNHG12 expression is relatively high in PTC tissues and cells. In-vivo /in-vitro experiments prove that SNHG12 can promote the proliferation and metastasis of PTC cells through influencing the Wnt/β -catenin signaling pathway. Show more
Keywords: Papillary thyroid carcinoma, lncRNA SNHG12, proliferation, invasion, metastasis, Wnt/β-catenin signaling pathway
DOI: 10.3233/CBM-170777
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 217-226, 2018
Authors: Wang, Yingchao | Jing, Wei | Ma, Weijie | Liang, Chunzi | Chai, Hongyan | Tu, Jiancheng
Article Type: Research Article
Abstract: BACKGROUND: Hepatocellular carcinoma (HCC) is the most common solid tumor in global range, with high degree of malignancy and poor prognosis. But the relationship between the expression of GAS5-AS1 and HCC is not documented. This study aimed to profile GAS5-AS1 expression signature and then to explore its clinical significance in HCC. METHODS: Quantitative real-time PCR (RT-qPCR) was performed to detect the expression of GAS5-AS1 in 83 pairs of HCC surgical tissues and adjacent normal liver tissues. We also performed RT-qPCR on plasma samples of 156 patients and 58 healthy controls. RESULTS: We found that GAS5-AS1 …was down-regulated in HCC tissues (P < 0.01). Correlation analysis showed that the expression of GAS5-AS1 was notably associated with differentiation (High/Moderate vs Low, P = 0.031), tumor-node-metastasis (TNM) stage (I∼ II vs III∼ IV, P = 0.020) and glucose levels (< 6.2 vs ≧ 6.2, P = 0.047) in HCC patients. The overall survival analysis showed that patients with lower GAS5-AS1 expression had a relatively poor prognosis. Univariate and multivariate analysis elaborated that GAS5-AS1 was an independent prognostic factor for HCC patients. The area under the ROC (AUC ROC ) demonstrated that GAS5-AS1 presented a high accuracy (AUC = 0.824, 95% CI: 0.741–0.906) for distinguishing HCC from the cirrhosis. When differentiating HCC cases with AFP < 200 ng/ml from the cirrhosis and hepatitis B whose AFP levels were also below 200 ng/ml, GAS5-AS1 had the high sensitivity (89.5%, 89.5%, respectively). CONCLUSIONS: GAS5-AS1 could be considered as a potential prognostic and diagnostic marker in HCC. However, the potential clinical application value of GAS5-AS1 still needs to be further illustrated. Show more
Keywords: Hepatocellular carcinoma, long non-coding RNA, GAS5-AS1, prognosis, diagnosis
DOI: 10.3233/CBM-170781
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 227-236, 2018
Authors: Wang, Yu | Jiang, Xiaorong | Wang, Shasha | Yu, Haixia | Zhang, Tingting | Xu, Shuan | Li, Wenlong | He, Ellen | Skog, Sven
Article Type: Research Article
Abstract: BACKGROUND: People with biomarkers above cut-off values normally have higher risk to develop pre-malignancies and malignancies. OBJECTIVE: Here we investigate if serological TK1 protein (STK1p), AFP, CEA and PSA below cut-off values predict development of pre-cancer. METHODS: The mean values and the concentration distribution of STK1p, AFP, CEA and PSA were determined in a cohort of 56,178 persons participating a health screening group, consist of people with non-tumor diseases, pre-malignancy and diseases associated with the risk process of malignancy. A health disease-free group (n = 428) was selected among …the 56,178 participants and used as controls. RESULTS: The STK1p below cut-off value (⩽ 2 pM) showed partly (51.6%) an almost normal concentration distribution and partly (43.9%) an extensive tail in the health screening group, which was not found in the disease-free group. Due to the extensive tail in the distribution, the mean value of STK1p increased significantly (p = 0.0001) from 0.38 ± 0.30 pM in the health disease-free group to 0.69 ± 0.55 pM in the group below the cut-off value. No significantly differences in the concentration distribution and the mean values among gender and ages were observed. On the other hand, there were no difference in the concentration distributions and the mean values of AFP, CEA and PSA between the health disease – free group and the group below cut-off values, as well as between gender and ages. Of interest, the elevated mean value of STK1p of the group below the cut-off value was correlated to pre-malignancy and diseases associated with the risk process of malignancy in liver and prostate. No such correlations were found with AFP, CEA and PSA. CONCLUSION: STK1p is a potential proliferating biomarker for early discover of persons in the risk to develop or already have pre-malignancies or diseases associated with the risk process of malignancy. Show more
Keywords: Thymidine kinase 1 (TK1), serum thymidine kinase 1 (STK1p), AFP, CEA, PSA, pre-malignancy
DOI: 10.3233/CBM-170846
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 237-247, 2018
Authors: Lu, Rongzhao | Zhang, Jie | Zhang, Wei | Huang, Yanhua | Wang, Ningxia | Zhang, Qing | Qu, Shaohua
Article Type: Research Article
Abstract: BACKGROUND: Long noncoding RNA HOTAIR has been detected in the serum of patients with various malignances and may be served as novel biomarker for diagnosis and prognosis prediction of breast cancer. However, the value of circulating HOTAIR to predict the response to neoadjuvant chemotherapy (NAC) remains unclear. OBJECTIVE: In the present study, we analyzed whether pretreatment circulating HOTAIR levels predict the response to NAC and investigated prognostic impact of circulating HOTAIR on disease-free survival (DFS) in breast cancer patients treated with NAC. METHODS: Circulating HOTAIR levels in the serum of 112 breast cancer …patients before NAC were measured using quantitative real-time PCR. The correlation of circulating HOTAIR with the clinicopathologic status and the response to NAC were analyzed. Kaplan-Meier survival analysis and log-rank test were used to estimate the DFS. RESULTS: In 112 serum samples obtained before NAC, high circulating HOTAIR was associated with larger tumor size, more positive lymph nodes as well as more distant metastasis. However, there was no significant correlation between the circulating HOTAIR levels and age, Ki67 status or hormone receptor. Furthermore, patients with high circulating HOTAIR achieved less clinical response as well as pathologic complete response than those with low circulating HOTAIR (p < 0.05). The Kaplan-Meier survival curve with a median follow-up of 48 months demonstrated that patients with high circulating HOTAIR expression had a worse disease-free survival than those with low circulating HOTAIR (log-rank p = 0.012). CONCLUSIONS: High circulating HOTAIR level correlates with less response to neoadjuvant chemotherapy as well as a worse prognosis in breast cancer patients. Therefore, the present study provides a favorable basis to use circulating HOTAIR as a predictor of neoadjuvant chemotherapy response. Show more
Keywords: Circulating HOTAIR, breast cancer, neoadjuvant chemotherapy
DOI: 10.3233/CBM-170874
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 249-256, 2018
Authors: Akinbo, David Bolaji | Onyeaghala, Augustine A. | Emomidue, Jennifer Ochuko | Ogbhemhe, Stephanie Okhuriafe | Okpoli, Henry Chijindu
Article Type: Research Article
Abstract: BACKGROUND: The Indian borage (Plectranthus amboinicus ) also called Oregano contains many effective antioxidants, which includes caffeic acid, rosmarinic acid and flavonoids. It has been employed in traditional medicine for its several health benefits including the prevention and cure of many debilitating diseases. Anti-inflammatory properties of Plectranthus amboinicus grown within this environment have not been adequately explored. OBJECTIVE: The protective and therapeutic effects of Oregano against endotoxaemia and inflammation were evaluated using lipopolysaccharide (LPS)-induced rat models. MATERIALS AND METHODS: A total of 30 Wistar rats were randomly selected for this study and …divided into six groups, with each group having 5 rats. Inflammation was induced on appropriate animal groups using LPS injection at a concentration of 4 mg/kg. Aqueous leaf extract of Indian borage was administered orally in four doses (100 mg/kg, 200 mg/kg, 400 mg/kg post-LPS exposure and 150 mg/kg pre-LPS exposure) to respective treatment rat groups. Haematological profile, toxicity profile of liver and kidney and levels of biomarkers of inflammation were assayed using standard methods. RESULTS: Rats injected with LPS showed severe anaemia and marked leucopoenia with significant decrease in monocytes compared to the control group (p < 0.05). There was increased expression of interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α ) (p < 0.05) in the peripheral circulation of rats exposed to LPS. Treatment with Indian borage significantly (p < 0.05) reduced the toxic effects in the LPS-treated animals and attenuated the increase in the expression of circulating proinflammatory cytokines; tumor necrosis factor alpha (TN-Fα ) and interleukin-8 (IL-8) caused by LPS. Indian borage pretreatment also significantly (p < 0.05) counteracted the associated haematological dyscrasias caused by exposure to LPS. The extract elicited a significant protective effect on the kidney and liver as evidenced by the decreased renal markers and hepatic enzyme activities when compared with the control. The extract demonstrated protective and suppressive role against the overexpression of inflammatory mediators by ameliorating the induced inflammation and endotoxaemic conditions in the affected rat groups thereby validating its folkloric use. CONCLUSION: Our study thus reveals that the extract might be an active, natural and non-toxic drug lead against endotoxaemia-induced inflammation and toxicity. Show more
Keywords: Anti-inflammatory, haematological indices, Indian borage, lipopolysaccharide, phytochemical constituents
DOI: 10.3233/CBM-170893
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 257-265, 2018
Authors: Liu, Qingyun | Xiang, Ying | Yuan, Shuai | Xie, Weijia | Li, Chengying | Hu, Zeyao | Wu, Na | Wu, Long | Yu, Zubin | Bai, Li | Li, Yafei
Article Type: Research Article
Abstract: BACKGROUND: Biomarker studies revealed important clinical significance of exosome for cancer patients. However, there is currently no consensus on exosome quantification methods. METHODS: Bicinchoninic acid (BCA) method, acetylcholinesterase (AChE) method and nanoparticle tracking analysis (NTA) were utilized to quantify 20 plasma exosome samples, and interrelations between these three methods were explored. Associations of plasma exosome levels with characteristics and prognosis of 208 non-small-cell lung cancer (NSCLC) patients were investigated. RESULTS: Results of the three methods for exosome quantification were significantly correlated with each other. Correlation coefficient between AChE and NTA (r = …0.79, P < 0.001) was greater than that between BCA and NTA (r = 0.64, P = 0.003). Plasma exosome levels of 208 NSCLC patients were then quantified with AChE method. Exosome level was significantly associated with tumour stage (P < 0.001) and the history of chronic obstructive pulmonary disease (P = 0.023). Cox proportional hazard analysis demonstrated that higher exosome level was independently associated with poorer overall survival (P = 0.033; hazard ratio = 1.72, 95% confidence interval: 1.05–2.83). CONCLUSIONS: Plasma exosome level correlates with tumor stage and the history of chronic obstructive pulmonary disease, and may serve as a prognostic factor for NSCLC. Show more
Keywords: Non-small-cell lung cancer, exosome, quantification, prognosis, biomarker
DOI: 10.3233/CBM-170955
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 267-274, 2018
Authors: Zhu, Zunwei | Xu, Lieyu | Wan, Yong | Zhou, Jie | Fu, Donghui | Chao, Haichao | Bao, Kunwang | Zeng, Tao
Article Type: Research Article
Abstract: Bladder cancer is derived from bladder mucosa and is the most common malignant tumor in urinary system. Long non-coding RNA (lnc-RNA) has high tissue specificity and can participate in cell proliferation and differentiation at various levels, and plays critical roles in occurrence of malignant tumors. This study aims to investigate the suppression of E-cadherin expression by lnc-RNA H19 to enhance bladder cancer metastasis. qRT-PCR was applied to analyze differential expression of lnc-RNA H19 in different bladder cancer tissues and tumor adjacent tissues. Patients clinical data were collected to analyze the correlation between H19 expression level and patient’s clinical stage, …tumor metastasis. RNA interference was employed to examine the effect of H19 on E-cadherin expression. The regulation of cancer metastasis was investigated on an animal model. H19 expression level was significantly higher in bladder cancer tissue compared to adjacent tissues (p < 0.05), and is correlated with advanced clinical stage (p < 0.05). In those metastatic patients, H19 expression level is significantly higher than those without metastasis (p < 0.05). RNA interference is applied to knockdown H19 expression in bladder cancer cell, and found potentiated E-cadherin expression (p < 0.05), accompanied with weakened metastatic potency (p < 0.05). H19 expression is up-regulated in bladder cancer, and is probably related with cancer clinical stage and metastasis. Cell transfection reveals up-regulation of E-cadherin expression in bladder cancer cells when H19 expression is suppressed, accompanied with weakened metastasis potency. Show more
Keywords: Bladder cancer, lnc-RNA-H19, E-cadherin, tumor metastasis
DOI: 10.3233/CBM-170998
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 275-281, 2018
Authors: Liu, Lin | Meng, Tao | Yang, Xin-Hui | Sayim, Parhat | Lei, Cheng | Jin, Bo | Ge, Lei | Wang, Hai-Jiang
Article Type: Research Article
Abstract: BACKGROUND: LncRNA and microRNA play an important role in the development of human cancers; they can act as a tumor suppressor gene or an oncogene. LncRNA GAS5, originating from the separation from tumor suppressor gene cDNA subtractive library, is considered as an oncogene in several kinds of cancers. The expression of miR-221 affects tumorigenesis, invasion and metastasis in multiple types of human cancers. However, there’s very little information on the role LncRNA GAS5 and miR-221 play in CRC. Therefore, we conducted this study in order to analyze the association of GAS5 and miR-221 with the prognosis of CRC and …preliminary study was done on proliferation, metastasis and invasion of CRC cells. In the present study, we demonstrate the predictive value of long non-coding RNA GAS5 (lncRNA GAS5) and mircoRNA-221 (miR-221) in the prognosis of colorectal cancer (CRC) and their effects on CRC cell proliferation, migration and invasion. METHODS: One hundred and fifty-eight cases with CRC patients and 173 cases of healthy subjects that with no abnormalities, who’ve been diagnosed through colonoscopy between January 2012 and January 2014 were selected for the study. After the clinicopathological data of the subjects, tissue, plasma and exosomes were collected, lncRNA GAS5 and miR-221 expressions in tissues, plasma and exosomes were measured by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The diagnostic values of lncRNA GAS5 and miR-221 expression in tissues, plasma and exosomes in patients with CRC were analyzed using receiver operating characteristic curve (ROC). Lentiviral vector was constructed for the overexpression of lncRNA GAS5, and SW480 cell line was used for the transfection of the experiment and assigned into an empty vector and GAS5 groups. The cell proliferation, migration and invasion were tested using a cell counting kit-8 assay and Transwell assay respectively. RESULTS: The results revealed that LncRNA GAS5 was upregulated while the miR-221 was downregulated in the tissues, plasma and exosomes of patients with CRC. The results of ROC showed that the expressions of both lncRNA GAS5 and miR-221 in the tissues, plasma and exosomes had diagnostic value in CRC. While the LncRNA GAS5 expression in tissues, plasma and exosomes were associated with the tumor node metastasis (TNM) stage, Dukes stage, lymph node metastasis (LNM), local recurrence rate and distant metastasis rate, the MiR-221 expression in tissues, plasma and exosomes were associated with tumor size, TNM stage, Dukes stage, LNM, local recurrence rate and distant metastasis rate. LncRNA GAS5 and miR-221 expression in tissues, plasma and exosomes were found to be independent prognostic factors for CRC. Following the overexpression of GAS5, the GAS5 expressions was up-regulated and miR-221 expression was down-regulated; the rate of cell proliferation, migration and invasion were decreased. Show more
DOI: 10.3233/CBM-171011
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 283-299, 2018
Authors: Guo, Tao | Zhao, Shilei | Li, Zhuoshi | Li, Fengzhou | Li, Jinxiu | Gu, Chundong
Article Type: Research Article
Abstract: BACKGROUND: Patients with small (⩽ 2 cm) invasive lung adenocarcinoma are at high risk of poor prognosis and disease recurrence after complete surgical resection. Therefore, identification of high-risk individuals from these patients emerges as an urgent problem. Elevated MACC1 expression predicts a poor prognosis in multiple types of cancer that are independent of TNM staging. This study investigated the prognostic value of MACC1 expression in patients with small invasive lung adenocarcinoma. OBJECTIVE: The current study aimed to evaluate the relationship between MACC1 expression in patients’ tumor tissue and prognosis in small invasive lung …adenocarcinoma. METHODS: The records of 131 patients with small invasive lung adenocarcinoma who underwent complete surgical resection were reviewed. The MACC1 expression was detected by immunohistochemical staining in all specimens. Meanwhile, western blot and real-time quantitative PCR were used to examine the expression level of MACC1 in human lung adenocarcinoma cell lines. The effect of clinicopathological risk factors on patients’ survival was analyzed using the Kaplan-Meier approach and multivariable Cox models. RESULTS: Elevated MACC1 expression was observed in 53 (40.5%) specimens, and in A549, H358, H460 and H322 lung adenocarcinoma cell lines. MACC1 overexpression was associated with differentiation (P = 0.005) and blood vessel invasion (P = 0.001). Compared with low MACC1 expression, elevated MACC1 expression was associated with significantly shorter overall survival (odds ratio = 6.515; 95% confidence interval: 1.382–30.721; P = 0.018) and disease-free survival (odds ratio = 3.270; 95% confidence interval: 1.117–9.569; P = 0.031). Multivariate analyses demonstrated high MACC1 expression is an independent risk factor of worse overall survival (odds ratio = 5.684; 95% confidence interval: 1.145–28.210; P = 0.034) and disease-free survival (odds ratio = 4.667; 95% confidence interval: 1.372–15.877; P = 0.014). CONCLUSION: MACC1 is an independent prognostic marker in patients with small invasive lung adenocarcinoma after complete surgical resection. Differential outcomes are associated with MACC1 expression level. Show more
Keywords: MACC1, lung adenocarcinoma, prognosis
DOI: 10.3233/CBM-171017
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 301-310, 2018
Authors: Lv, Jia | Yang, Huyin | Wang, Xiaodong | He, Ruixing | Ding, Lianshu | Sun, Xiaoyang
Article Type: Research Article
Abstract: AIMS: To evaluate the prognostic and clinicopathological features of glioma with BRMS1L expression. METHODS: Total 120 glioma samples were obtained as discovery cohort. CGGA, GSE and TCGA datasets were obtained as validation sets. Furthermore, Kaplan-Meier survival and multivariate Cox analysis were used to evaluate the survival distributions. Moreover, the functional role of BRMS1L was also analyzed by transwell assay. RESULTS: In the discovery cohort, decreased BRMS1L expression was significantly associated with high-grade glioma as well as the higher mortality in survival analysis (log-rank test, p < 0.01). And the …three validation cohorts showed the similar results. Furthermore, BRMS1L act as an independent prognostic factor in glioblastoma patients. Additionally, functional assay showed that ectopic of BRMS1L suppressed glioma cells’ invasion. CONCLUSION: BRMS1L plays as an anti-oncogene in GBM and indicates a new potential therapeutic target. Show more
Keywords: Glioma, BRMS1L, prognostic, invasion
DOI: 10.3233/CBM-171019
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 311-316, 2018
Authors: Molina-Ortiz, Dora | Torres-Zárate, Carmen | Cárdenas-Cardós, Rocío | Palacios-Acosta, José Martin | Hernández-Arrazola, Daniel | Shalkow-Klincovstein, Jaime | Díaz-Díaz, Erick | Vences-Mejía, Araceli
Article Type: Research Article
Abstract: BACKGROUND: Intratumoral up-regulation of genes coding for drug transporters and metabolizing enzymes, such as MDR1 and CYP3A4, after chemotherapy are linked to cancer drug resistance. However their expression in primary soft tissue sarcomas (STS) prior to drug treatment and their role in innate resistance remain unclear. OBJECTIVE: The aim of this study was characterize MDR1 and CYP3A4 expression pattern before to chemotherapy and its clinical implication in pediatric STS. METHODS: In this prospective study we analyzed MDR1 and CYP3A4 mRNA expression in both normal and tumor tissues from 28 newly diagnosed STS pediatric …and then compared with patients’ clinical-pathological data, including chemotherapy response. RESULTS: Our data showed that the expression of the MDR1 gene was significantly higher in malignant tissue than in the normal tissues of patients with STS. In addition, high MDR1 expression was significantly associated with local advances, as well as poor response to treatment. In contrast, CYP3A4 expression level was negligible in both tumoral and non-tumoral tissues. CONCLUSIONS: These results suggest that a significant mRNA level of MDR1 gene was intrinsically present in STS before exposure to chemotherapeutic drugs, suggesting that MDR1 may be important contributors of innate chemoresistance of this tumor type. Show more
Keywords: Soft tissue sarcomas, chemoresistance, MDR1, CYP3A4, mRNA expression level
DOI: 10.3233/CBM-171027
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 317-324, 2018
Authors: Babińska, Anna | Pȩksa, Rafał | Świa̧tkowska-Stodulska, Renata | Wiśniewski, Piotr | Sworczak, Krzysztof
Article Type: Research Article
Abstract: BACKGROUND: The role of adopokines in adrenal tumors’ hormonal activity remains unclear. Obesity may induce arterial hypertension, disorders of carbohydrate metabolism, and is a risk factor of cardiovascular disease. In patients with subclinical hormone secretion by the adrenal cortex or medulla the risk of metabolic disease is increased. OBJECTIVE: Authors of this retrospective study selected 78 patients with subclinical hormone secretion out of all adrenal incidentaloma patients hospitalized in the Department of Endocrinology and Internal Medicine between 1995 and 2014. METHODS: The analyzed group comprised of 38 subclinical Cushing’s syndrome (SCS), 40 incidentally …discovered pheochromocytoma (PHEO) and 42 patients operated due to an adrenal tumor without pathological hormonal activity. Expression of adiponectin (AdipoR1, AdipoR2) and leptin (Ob-R) receptors in adrenal tumors was assessed in relation to body mass index (BMI) and hormonal activity. RESULTS: We found statistically significant negative correlations between BMI and expression of all examined receptors in SCS patients (AdipoR1: p = 0.032; AdipoR2: p < 0.001; leptin Ob-R: p = 0.001). In PHEOs, BMI correlated negatively only with AdipoR2 (p = 0.014). CONCLUSIONS: Data obtained show that the most significant factor associated with the expression of AdipoR1, AdipoR2 and leptin Ob-R receptors in the adrenal tumor tissue is BMI, not their hormonal activity. Show more
Keywords: AdipoR1, AdipoR2 and Leptin Ob-R receptors, BMI, adrenal tumors
DOI: 10.3233/CBM-171049
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 325-332, 2018
Authors: Hughes, Nicholas P. | Xu, Lingyun | Nielsen, Carsten H. | Chang, Edwin | Hori, Sharon S. | Natarajan, Arutselvan | Lee, Samantha | Kjær, Andreas | Kani, Kian | Wang, Shan X. | Mallick, Parag | Gambhir, Sanjiv Sam
Article Type: Research Article
Abstract: BACKGROUND AND OBJECTIVE: To monitor therapies targeted to epidermal growth factor receptors (EGFR) in non-small cell lung cancer (NSCLC), we investigated Peroxiredoxin 6 (PRDX6) as a biomarker of response to anti-EGFR agents. METHODS: We studied cells that are sensitive (H3255, HCC827) or resistant (H1975, H460) to gefitinib. PRDX6 was examined with either gefitinib or vehicle treatment using enzyme-linked immunosorbent assays. We created xenograft models from one sensitive (HCC827) and one resistant cell line (H1975) and monitored serum PRDX6 levels during treatment. RESULTS: PRDX6 levels in cell media from sensitive cell lines increased significantly …after gefitinib treatment vs. vehicle, whereas there was no significant difference for resistant lines. PRDX6 accumulation over time correlated positively with gefitinib sensitivity. Serum PRDX6 levels in gefitinib-sensitive xenograft models increased markedly during the first 24 hours of treatment and then decreased dramatically during the following 48 hours. Differences in serum PRDX6 levels between vehicle and gefitinib-treated animals could not be explained by differences in tumor burden. CONCLUSIONS: Our results show that changes in serum PRDX6 during the course of gefitinib treatment of xenograft models provide insight into tumor response and such an approach offers several advantages over imaging-based strategies for monitoring response to anti-EGFR agents. Show more
Keywords: Serum biomarkers, gefitinib, EGFR, NSCLC, proteomics, ELISA
DOI: 10.3233/CBM-171149
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 333-344, 2018
Authors: Takeshita, Takashi | Yamamoto, Yutaka | Yamamoto-Ibusuki, Mutsuko | Tomiguchi, Mai | Sueta, Aiko | Iwase, Hirotaka
Article Type: Research Article
Abstract: PURPOSE: Plasma and serum cell-free DNA (cfDNA) are useful sources of tumor DNA, but comparative investigations of the tumor mutational status between them are rare. METHODS: we performed droplet digital PCR assay for representative hotspot mutations in metastatic breast cancer (MBC) (ESR1 and PIK3CA ) in serum and plasma cfDNA concurrently extracted from the blood of 33 estrogen receptor-positive MBC patients. RESULTS: ESR1 mutations in plasma cfDNA were found in 7 of the 33 patients; ESR1 mutations in serum cfDNA were detected in only one out of 7 patients with ESR1 mutations in plasma …cfDNA. PIK3CA exon 9 and exon 20 mutations in plasma cfDNA were found in 3 and 7 out of the 33 patients, respectively; PIK3CA exon 9 mutations in serum cfDNA were detected in 2 out of 3 patients with PIK3CA exon 9 mutations in plasma cfDNA; PIK3CA exon 20 mutations in serum cfDNA were detected in 2 out of 7 patients with PIK3CA exon 20 mutations in plasma cfDNA. CONCLUSIONS: Here we show the higher frequency of ESR1 and PIK3CA mutations in the plasma than in the serum in 33 MBC patients; therefore, serum samples should not be considered the preferred source of cfDNA. Show more
Keywords: Metastatic breast cancer, serum cell-free DNA, plasma cell-free DNA, ESR1 mutation, PIK3CA mutation, digital PCR
DOI: 10.3233/CBM-171161
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 345-350, 2018
Authors: Liberati, Daniela | Marzinotto, Ilaria | Brigatti, Cristina | Dugnani, Erica | Pasquale, Valentina | Reni, Michele | Balzano, Gianpaolo | Falconi, Massimo | Piemonti, Lorenzo | Lampasona, Vito
Article Type: Research Article
Abstract: BACKGROUND: Sensitive and specific biomarkers of Pancreatic Ductal Adenocarcinoma (PDAC) are desperately needed to allow early diagnosis and improve patient’s survival. Ezrin autoantibodies were recently described as present in 93% of PDAC patients and 40% of healthy subjects who later developed PDAC. However, another prospective study failed to replicate these findings. Both studies were based on the use of a solid phase ELISA immunoassay. OBJECTIVE: We aimed at re-evaluating the usefulness of Ezrin autoantibodies as PDAC biomarkers using the Luciferase Immuno Precipitation System (LIPS), an alternative immunoassay format that found successful application for the measurement of …autoantibodies against pancreatic autoantigens. METHODS: We produced a Nanoluciferase™ tagged Ezrin (NLuc-Ezrin). NLuc-Ezrin was then used as antigen in LIPS to test for Ezrin autoantibodies patients affected by PDAC (n = 40), other pancreatic diseases (OPD, n = 50), and healthy controls (n = 60). RESULTS: Overall, binding in liquid phase to Ezrin by serum antibodies was rare and low titer. Furthermore, we did not find statistically significant differences in the prevalence of Ezrin autoantibodies between patients affected by either PDAC or OPD compared to control. CONCLUSIONS: Our results do not confirm the usefulness of Ezrin autoAbs as biomarker of PDAC. Show more
Keywords: PDAC, TAA, biomarker, autoantibody, LIPS
DOI: 10.3233/CBM-181218
Citation: Cancer Biomarkers, vol. 22, no. 2, pp. 351-357, 2018
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