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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: Wang, Juan | Zhang, Shufang | Ni, Weihua | Zhai, Xiaoyu | Xie, Fei | Yuan, Hongyan | Gao, Sujun | Tai, Guixiang
Article Type: Research Article
Abstract: BACKGROUND: Mucin 1 (MUC1), as an oncogene, plays an important role in the diagnosis of lung cancer. OBJECTIVE: To establish a double-antibody sandwich enzyme-linked immune sorbent assay (ELISA) kit for the detection of serum MUC1 in lung cancer patients. METHODS: Commercial mouse anti-human MUC1 monoclonal antibody and rabbit anti-human MUC1 polyclonal antibody were used to construct a double-antibody sandwich ELISA kit. The serum MUC1 levels in peripheral blood of lung disease patients and healthy individuals were detected by the double-antibody sandwich ELISA kit and CA15-3 kit, respectively. RESULTS: A double-antibody …sandwich ELISA kit was successfully constructed, and the sensitivity was up to 0.5 μ g/l. The cut-off value for the serum MUC1 levels in the peripheral blood was 1.98 μ g/l, the sensitivity was 62.5%, the specificity was 100% and the Youden index was 0.6250 when detected by the double-antibody sandwich ELISA kit, while the sensitivity was 18.75%, the specificity was 100% and the Youden index was 0.1875 when detected by CA15-3 kit. CONCLUSION: The double-antibody sandwich ELISA kit is superior to the CA15-3 kit in the detection of serum MUC1 in lung cancer patients, suggesting an attractive applying of the double-antibody sandwich ELISA kit in the early diagnosis of lung cancer. Show more
Keywords: MUC1, anti-MUC1 polyclonal antibody, ELISA, CA15-3, lung cancer
DOI: 10.3233/CBM-160649
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 369-376, 2016
Authors: Li, Shu-Xia | Yang, Yan-Qi | Jin, Li-Jian | Cai, Zhi-Gang | Sun, Zheng
Article Type: Research Article
Abstract: INTRODUCTION: The aim of this study was to detect the survivin, carcinoembryonic antigen (CEA) and ErbB2 in the saliva, serum and local tumor-exfoliated cells of oral squamous cell carcinoma (OSCC) patients, for providing reliable tumor markers for the early detection of oral malignant cancer. MATERIALS AND METHODS: The saliva, serum, and local tumor-exfoliated cell samples of 26 OSCC patients without chemotherapy and 10 non-cancer patients were collected in Department of Oral and Maxillofacial Surgery, School of Stomatology, Peking University. The contents of survivin, CEA and ErbB2 using were detected usingenzyme-linked immunosorbent assay. …RESULTS: The survivin and CEA levels in saliva and local tumor-exfoliated cells of OSCC patients were significantly higher than those in the non-cancer patients (P < 0.05), but there was no significant difference in the content of the above factors in the serum sample between two groups. There was no significant difference in the ErbB2 content in the saliva, serum or local tumor-exfoliated cells between two groups. CONCLUSION: Survivin and CEA levels are significantly increased in the saliva and local tumor-exfoliated cells in OSCC patients, and they can be used as reliable markers for the early detection of oral malignant cancer. Show more
Keywords: Oral squamous cell carcinoma, detection, survivin, CEA, ErbB2
DOI: 10.3233/CBM-160651
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 377-382, 2016
Authors: Yang, Hai-Su
Article Type: Research Article
Abstract: BACKGROUND: Hematopoietic malignancies are a group of blood cell disorders characterized by abnormal hematopoietic proliferation. OBJECTIVE: The identification of specific clinicopathologic characteristics and tumor-related gene status provides critical information on potential therapeutic targets. METHODS: The specimens were tested with immunohistochemistry, flow cytometry, RT-PCR and fragment analysis. RESULTS: In this study, a patient with a long history of tobacco use was reported with a diagnosis of simultaneous low-grade B-cell lymphoproliferative disorder (LPD) and myeloproliferative neoplasm (MPN). Mutational analysis revealed that JAK2 V617F mutation and CALR mutation with 52bp deletion were present …in this patient. CONCLUSION: These results suggest that lymphoproliferative and myeloproliferative neoplasms may coexist, although the pathogenetic mechanism of coexisting hematologic requires further investigation. Additionally, the data indicate that JAK2 V617F and CALR mutations are not mutually exclusive and the actual frequency of simultaneous JAK2 V617F and CALR mutations is unknown. Whether the coexistence of these mutations imposes any biological or clinical significance awaits further investigation. Show more
Keywords: Lymphoproliferative neoplasm, MPNs, JAK2, CALR
DOI: 10.3233/CBM-160652
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 383-389, 2016
Authors: Maden, Muhammet | Pamuk, Omer Nuri | Pamuk, Gulsum Emel
Article Type: Research Article
Abstract: BACKGROUND: Apelin/APJ system regulates angiogenesis and is overexpressed in some malignancies. Apelin can induce lymphangiogenesis and lymph node metastasis. OBJECTIVE: We evaluated apelin levels in multiple myeloma (MM) and non-Hodgkin lymphoma (NHL); and analyzed the association between apelin levels and clinical findings. METHODS: We included consecutive 29 MM, 31 NHL patients, and 19 healthy controls. Patients' demographic and clinical features, treatment modalities, and responses were recorded from hospital records. Plasma apelin was determined by enzyme-linked immunosorbent assay (ELISA). RESULTS: MM patients had significantly higher plasma apelin level than NHL …and healthy control groups (p< 0.001). Apelin level in NHL group was similar to controls (p> 0.05). ROC curve analysis showed that the area under the curve value for apelin level in MM was 0.842 ng/ml (95%CI: 0.739-0.945, p< 0.001). Plasma apelin level ≥ 0.827 ng/ml had 76% sensitivity and 86% specificity for the diagnosis of MM. Multivariate Cox regression analysis showed that MM patients with high apelin level had better prognosis and patients with advanced stage of disease (ISS-3) had significantly poor prognosis when compared to others. In the MM group, apelin level correlated negatively with LDH (r = -0.39, p= 0.038). CONCLUSIONS: In MM, plasma apelin level was significantly higher than in NHL and control groups. Apelin could be playing a role in MM pathogenesis; and apelin level could be used as a diagnostic and prognostic biomarker in MM. Show more
Keywords: Multiple myeloma, non-Hodgkin lymphoma, apelin, survival
DOI: 10.3233/CBM-160654
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 391-396, 2016
Authors: Yao, Hongliang | Yang, Zhulin | Liu, Ziru | Miao, Xiongying | Yang, Leping | Li, Daiqiang | Zou, Qiong | Yuan, Yuan
Article Type: Research Article
Abstract: OBJECTIVE: Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant tumor with metastasis in most patients at diagnosis. The molecular mechanisms associated with its high malignancy have not been fully elucidated. This study investigated the clinicopathological significances of GPC3 and KRT19 expression in PDAC. METHODS: GPC3, KRT19, and CA19-9 protein expression were measured by immunohistochemistry. RESULTS: GPC3 and KRT19 protein levels were overexpressed in PDAC tumors compared to normal pancreatic tissues, benign pancreatic tissues, and peritumoral tissues (P< 0.01). The percentage of positive GPC3 and KRT19 expression were significantly higher in PDAC …patients with larger tumor size, poorly differentiated tumor, lymph node metastasis, invasion, and TNM stage III/IV disease than in patients with small tumor size, well-differentiated tumor, no lymph node metastasis and invasion, as well as TNM stage I/II stage disease (P< 0.05 or P< 0.01). Benign pancreatic lesions with positive GPC3 and KRT19 protein expression exhibited dysplasia or intraepithelial neoplasia. Kaplan-Meier survival analysis showed that PDAC patients with positive GPC3 and KRT19 expression survived significantly shorter than patients with negative GPC3 and KRT19 expression (P < 0.05 or P< 0.001). Cox multivariate analysis revealed that positive GPC3 and KRT19 expression were independent poor prognosis factors in PDAC patients. CONCLUSIONS: GPC3 and KRT19 overexpression are associated with carcinogenesis, progression, and poor prognosis in patients with PDAC and a valuable biomarker for diagnosis of PDAC. Show more
Keywords: Pancreatic ductal adenocarcinoma, dysplasia, pancreatic intraepithelial neoplasia, GPC3, KRT19, CA19-9, immunohistochemistry
DOI: 10.3233/CBM-160655
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 397-404, 2016
Authors: Ittel, Antoine | Zattara, Hélène | Chaix, Charlène | Michel, Gérard | Levy, Nicolas
Article Type: Research Article
Abstract: BACKGROUND: According to the World Health Organization (WHO), recurrent cytogenetic abnormalities define many specific groups of hematopoietic tumors of acute myeloid and lymphoblastic leukemia, and these abnormalities are often strongly associated with prognosis and sometimes require specific treatments. These rearrangements are commonly detected by conventional and molecular cytogenetic techniques. OBJECTIVE: Using an alternative method, we sought to highlight the presence of chromosomal rearrangements. METHODS: We applied molecular combing to detect and directly visualize gene fusions associated with balanced translocations found in acute leukemia. RESULTS: In patients harboring t(12;21)(p13;q22), we demonstrated …the presence of the fusion using specific probes covering the ETV6 and RUNX1 genes, with a positive result occurring due to the hybridization of the two probes to the same DNA fiber. Thanks to molecular combing, we also showed the presence of different breakpoints using these same probes. CONCLUSIONS: Using several probes that are specific to the most common genes involved in acute leukemia, molecular combing could be an interesting additional tool in acute leukemia diagnosis. Show more
Keywords: Molecular combing, leukemia, recurrent chromosomal abnormalities, translocation t(12;21)(p13;q22)
DOI: 10.3233/CBM-160656
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 405-409, 2016
Authors: Wƚodarczyk, Marcin | Kasprzyk, Jakub | Sobolewska-Wƚodarczyk, Aleksandra | Wƚodarczyk, Jakub | Tchórzewski, Marcin | Dziki, Adam | Dziki, Ƚukasz
Article Type: Research Article
Abstract: BACKGROUND: Rectal cancer is a major cause of death and an early diagnosis is crucial in decreasing mortality. Previous studies found a relation between chronic inflammation and increased risk of rectal cancer. It was shown that mean platelet volume (MPV) level might be a marker of subclinical inflammatory process in gastrointestinal tract. OBJECTIVE: To determinate whether MPV could be a useful biomarker of tumor progression in the rectal cancer. METHODS: One hundred and three patients with rectal cancer who underwent surgical resection of tumor were enrolled in the study. The control group consisted …of 98 healthy subjects. RESULTS: The association between MPV, tumor stage and clinical status were assessed. The analysis proved that pre-operative MPV level was significantly lower in rectal cancer vs. healthy individuals (10.65 ± 0.79 vs. 11.41 ± 0.76 fL; p < 0.001). Receiver-operating characteristic curve analysis suggested 11.3 as the cut-off value for MPV (sensitivity = 83%; specificity = 54%; AUC = 0.745). Surgical resection of tumor resulted in the increase of the MPV level with statistical significance (10.65 ± 0.79 fL vs. 11.21 ± 0.82 fL; p < 0.001). No relationship was found between the post-operative MPV level in cancer patients and control subjects. CONLUSION: MPV level may be potentially useful and easily available biomarker for monitoring subclinical inflammation related to rectal cancer and predicting tumor progression. Show more
Keywords: Biomarker, mean platelet volume, rectal cancer, tumor progression, inflammation
DOI: 10.3233/CBM-160657
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 411-417, 2016
Authors: Paik, E Sun | Shim, Minhee | Choi, Hyun Jin | Lee, Yoo-Young | Kim, Tae-Joong | Choi, Chel Hun | Lee, Jeong-Won | Kim, Byoung-Gie | Bae, Duk-Soo
Article Type: Research Article
Abstract: BACKGROUND: Epithelial ovarian cancer (EOC) is leading cause of death in gynecologic cancer, and finding prognostic factors is important for establishing treatment plans. OBJECTIVE: The aim of this study was to investigate the prognostic value of the multiplication of neutrophil and monocyte counts (MNM) in epithelial ovarian cancer (EOC). METHODS: Data were retrospectively collected from Samsung Medical Center for EOC patients treated from January 2002 to December 2012. MNM was determined by multiplying neutrophil and monocyte counts and dividing by 10,000. Sensitivity and specificity of markers were assessed using receiver operating characteristic curves. …RESULTS: We included 674 patients with EOC. For predicting overall survival (OS), the area under the curve for MNM was 0.607 (95% CI, 0.554-0.661) with sensitivity 55.2% and specificity 63.2% (cut-off value 197.40). The ability of MNM to determine OS was similar to that of the previously validated NLR and PLR. When the cohort was divided by cut-off values, poorer survival outcomes were observed in the group with higher MNM. Higher MNM was associated with advanced stage and presence of residual disease after primary treatment. CONCLUSIONS: Elevated pretreatment MNM is an independent predictor of poor survival and can be a useful biomarker in patients with EOC. Show more
Keywords: Monocytes, neutrophils, ovarian neoplasm, biological markers, prognosis
DOI: 10.3233/CBM-160658
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 419-425, 2016
Authors: Clancy, Cillian | Khan, Sonja | Glynn, Claire L. | Holian, Emma | Dockery, Peter | Lalor, Pierce | Brown, James A.L. | Joyce, Myles R. | Kerin, Michael J. | Dwyer, Roisin M.
Article Type: Research Article
Abstract: BACKGROUND: Cells release extracellular membrane vesicles including microvesicles known as exosomes. Exosomes contain microRNAs (miRNAs) however the full range within colorectal cancer cell secreted exosomes is unknown. OBJECTIVE: To identify the full range of exosome encapsulated miRNAs secreted from 2 colorectal cancer cell lines and to investigate engineering of exosomes over-expressing miRNAs. METHODS: Exosomes were isolated from HCT-116 and HT-29 cell lines. RNA was extracted from exosomes and microRNA array performed. Cells were engineered to express miR-379 (HCT-116-379) or a non-targeting control (HCT-116-NTC) and functional effects were determined. Exosomes secreted by engineered cells …were transferred to recipient cells and the impact examined. RESULTS: Microvesicles 40-100 nm in size secreted by cell lines were visualised and confirmed to express exosomal protein CD63. HT-29 exosomes contained 409 miRNAs, HCT-116 exosomes contained 393, and 338 were common to exosomes from both cell lines. Selected targets were validated. HCT-116-379 cells showed decreased proliferation (12-15% decrease, p < 0.001) and decreased migration (32-86% decrease, p < 0.001) compared to controls. HCT-116-379 exosomes were enriched for miR-379. Confocal microscopy visualised transfer of HCT-116-379 exosomes to recipient cells. CONCLUSIONS: Colorectal cancer cells secrete a large number of miRNAs within exosomes. miR-379 decreases cell proliferation and migration, and miR-379 enriched exosomes can be engineered. Show more
Keywords: Exosomes, microRNAs, colorectal cancer
DOI: 10.3233/CBM-160659
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 427-435, 2016
Authors: Yang, Zhulin | Li, Daiqiang | Liu, Ziru | Miao, Xiongying | Yang, Leping | Zou, Qiong | Yuan, Yuan
Article Type: Research Article
Abstract: This study investigated the KLF4 and BIRC7 protein expression in malignant and benign pancreatic tissues by immunohistochemical staining and the clinical and pathological significance of KLF4 and BIRC7 expression in PDAC. KLF4 expression was significantly lower, whereas BIRC7 expression was significantly higher in PDAC than that in peritumoral tissue, benign pancreatic lesions, and normal pancreatic tissue (P < 0.01). The percentage of positive BIRC7 and negative KLF4 expression was significantly lower in PDAC patients with well differentiated tumors, maximum tumor size < 3 cm, no lymph node metastasis, no invasion to the surrounding tissues and organs, and TNM stage I/II …stage disease than in patients with poorly differentiated tumor, maximum tumor size > 5 cm, lymph node metastasis, invasion to surrounding tissues and organs, and TNM stage III/IV disease (P < 0.05 or P < 0.01). Kaplan-Meier survival analysis showed that the differentiation, maximum tumor size, TNM stage, lymph node metastasis, invasion, negative KLF4 expression, and positive BIRC7 expression were significantly associated with the short survival of patients with PDAC (P < 0.05 or P < 0.01). Cox multivariate analysis revealed that positive BIRC7 expression and negative KLF4 expression were independent poor prognosis factors in PDAC patients. In conclusions, positive BIRC7 expression and negative KLF4 expression are associated with the progression of PDAC and poor prognosis in patients with PDAC. Show more
Keywords: Pancreatic ductal adenocarcinoma, chronic pancreatitis, pancreatic intraepithelial neoplasia, KLF4, BIRC7, immunohistochemistry
DOI: 10.3233/CBM-160660
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 437-444, 2016
Authors: Huang, Zhiliang | Ai, Zenan | Li, Nan | Xi, Haofeng | Gao, Xucan | Wang, Feng | Tan, Xiaojun | Liu, Haiying
Article Type: Research Article
Abstract: BACKGROUND: Over expression of galectin-3 (gal-3) has been associated with tumor invasion and distant metastases, but few reports investigated the relation between gal-3 expression and prognosis in stage II colon cancer. OBJECTIVE: We studied the expressions of gal-3, E-cadherin, and vimentin in stage II colon cancer to identify predictive factors of clinical outcome. METHODS: Clinical and laboratory data from 117 consecutive patients of stage II colon cancer during 2008-2010 were collected and analyzed retrospectively. Expressions of gal-3, E-cadherin, and vimentin in tumor tissue were investigated by immunohistochemistry. Potential correlations between these markers and …various clinicopathological parameters as well as clinical outcomes were studied. Human colon cancer cell line SW480 was used to test the epithelial-mesenchymal transition (EMT) inducing effects of gal-3 in vitro . RESULTS: High expression of tumoral gal-3 was associated with tumor size, poor differentiation and negatively related to low E-cadherin expression. Compare with adjacent normal colon tissue, most tumor tissues strongly expressed gal-3 and vimentin, but had lower E-cadherin expression. Univariate analysis showed that expressions of gal-3 and vimentin in tumor were predictors of tumor recurrence and overall survival. Multivariate analysis revealed that tumoral gal-3 expression was the only independent predictor of both tumor recurrence and overall survival after resection. Cell experiments and western blotting showed exogenous gal-3 could induce SW480 cells become more aggressive and express more hallmarks of EMT. CONCLUSIONS: Galectin-3 may be a useful marker for identification of poor prognosis in stage II colon cancer. Cell experiments and western blotting showed exogenous gal-3 could induce SW480 cells become more aggressive and express more hallmarks of EMT. Show more
Keywords: Galectin-3, E-cadherin, vimentin, colon cancer, prognosis
DOI: 10.3233/CBM-160661
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 445-455, 2016
Authors: Khan, Fatima | Vogel, Rachel I. | Diep, Gustave K. | Tuttle, Todd M. | Lou, Emil
Article Type: Research Article
Abstract: BACKGROUND: Appendiceal cancer is a rare malignancy. The optimal pathologic classification and prognostic factors for survival and treatment strategies remain poorly understood. OBJECTIVE: The aim of this retrospective cohort study was to determine prognostic factors, including markers of systemic inflammation, for survival in a cohort of patients with advanced appendiceal adenocarcinomas. METHODS: The study included patients with advanced appendiceal carcinoma that were treated between January 2006 and June 2012. The associations between age, gender, histopathologic subtype of appendiceal malignancy and treatment with heated intraperitoneal chemotherapy (HIPEC) and overall survival (OS) were assessed. The …relationship between various markers of inflammation (platelet-to-lymphocyte ratio, neutrophil-to-lymphocyte ratio) and OS was also evaluated. RESULTS: A total of 49 patients met eligibility criteria. Female gender and low-grade adenocarcinoma were associated with increased OS. These data suggest that the use of HIPEC treatment may also be associated with improved OS, but the difference was not statistically significant (HR = 0.37 [0.12-1.18], p = 0.09). We found no evidence of an association between markers of inflammation at diagnosis and OS. CONCLUSIONS: Histopathologic subtype and gender are associated with OS in patients with advanced appendiceal carcinoma. Baseline platelet levels, NLR, and PLR do not appear to be predictive of OS in this setting. Show more
Keywords: Appendiceal cancer, HIPEC, prognostic factors, platelet-to-lymphocyte ratio, neutrophil-to-lymphocyte ratio
DOI: 10.3233/CBM-160662
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 457-462, 2016
Authors: Wang, Lei | Ma, Hong | Zhu, Lixia | Ma, Liping | Cao, Lanting | Wei, Hui | Xu, Jumei
Article Type: Research Article
Abstract: OBJECTIVE: To investigate novel gene sets related to breast cancer (BC) using differential co-expression and differential expression (DECODE). METHODS: T statistics was used to quantify the degree of DE of each gene, and then Z was adopted to quantify the correlation difference between expression levels of two genes. Two optimal thresholds for defining substantial change in DE and DC were selected for each gene using chi-square maximization, and the corresponding gene was defined as the optimal gene. Based on the optimal thresholds, genes were categorized into four partitions with either high or low DC and DE …characteristics. Finally, we evaluated the functional relevance of a gene partition with high DE and high DC, and the gene set with best association was considered as the optimal functional gene set. RESULTS: The optimal thresholds for DC and DE were respective 2.254 and 1.616, and the optimal gene was UBE2Q2L. Based on the optimal thresholds, genes were divided into four partitions including HDE-HDC (875 genes), HED-LDC (8038 genes), LDE-HDC (678 genes), and LDE-LDC (10516 genes). The best associated gene set was ``fatty acid catabolic process'' with 34 HDC and HDE partitions. Among these partitions, UBE2Q2L attained the highest minimum FI gain of 18.973. CONCLUSION: UBE2Q2L and fatty acid catabolic process might be potentially useful signatures in diagnostic purposes for BC. Show more
Keywords: Breast cancer, differential co-expression and differential expression, functional information
DOI: 10.3233/CBM-160663
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 463-471, 2016
Authors: Lee, Deok Heon | Lee, Jae-Ho | Keum, Dong Yoon | Kim, Dae-Kwang
Article Type: Research Article
Abstract: BACKGROUND: The genetic alteration of mitochondrial DNA has been regarded as an important step in the development of several human tumors. OBJECTIVE: The purpose of this study was to identify frequency of mitochondrial microsatellite instability (mtMSI) and alterations in mitochondrial DNA copy number (mtCN) in pulmonary hamartoma. METHODS: DNA was isolated from tumor tissue and matched non-tumor tissue in 30 patients with pulmonary hamartoma. BAT 25 and 26 were used as nucleus MSI (nMSI) markers, and (C)n and (CA)n in D-loop were used as mtMSI markers. MtCNs were quantified using a competitive quantitative …real-time polymerase chain reaction. RESULTS: nMSI was detected in 5 patients (23.8%) and mtMSI was detected in 2 patients (9.5%) of total 21 hamartoma. There were 14 patients (46.7%), 2 patients (6.7%), and a further 14 patients (46.7%) in the decreased, no change, and increased mtCN groups, respectively. The mean relative mtCN were 0.4 ± 0.3 in the decreased and 3.9 ± 5.1 in the increased mtCN groups, respectively. CONCLUSIONS: nMSI was more frequently appeared than mtMSI in hamartomas, and we also found measurements of mtCNs in patients with pulmonary hamartoma to be extremely variable without any characteristic pattern. Show more
Keywords: Hamartoma, microsatellite instability, DNA copy number
DOI: 10.3233/CBM-160664
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 473-478, 2016
Authors: Orsaria, Maria | Londero, Ambrogio P. | Marzinotto, Stefania | Di Loreto, Carla | Marchesoni, Diego | Mariuzzi, Laura
Article Type: Research Article
Abstract: OBJECTIVE: To analyze the expression profile of placental type alkaline phosphatase (PLAP), cancer antigen 125 (CA125), and human epididymis protein 4 (HE4) in serous ovarian cancer and to correlate their expression with the tumor aggressiveness and progression. METHODS: Retrospective study considering a tissue microarray of 82 women affected by ovarian serous cancer. Protein expression was assessed by immunohistochemistry on ovarian serous cancer tissue samples. Immunohistochemical staining was semiquantitatively evaluated as H-score. RESULTS: Median H-score values were lower for PLAP, 1 (IQR 0-4) than CA125, 10 (IQR 6-12) or HE4, 8 (IQR 5-12). Even …if PLAP was less expressed in the cells of serous ovarian cancer than CA125 or HE4 it was relatively more expressed in the fourth quartile of its H-score distribution among cases with low CA125 or HE4 expression. Furthermore, PLAP and HE4 high expression resulted to be significantly correlated with a better prognosis. CONCLUSIONS: PLAP could be an additional marker for early detection of serous ovarian carcinoma, together with the established CA125 and HE4. In addition, PLAP expression is correlated with prognosis, giving, in this way, an additional tool for improving treatment approach. Show more
Keywords: PLAP, HE4, CA125, survival, prognostic factors, ovarian serous cancer
DOI: 10.3233/CBM-160665
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 479-486, 2016
Authors: Juodzbalys, Gintaras | Kasradze, David | Cicciù, Marco | Sudeikis, Aurimas | Banys, Laurynas | Galindo-Moreno, Pablo | Guobis, Zygimantas
Article Type: Research Article
Abstract: INTRODUCTION: Nearly half of the head and neck cancer cases are diagnosed in late stages. Traditional screening modalities have many disadvantages. The aim of the present article was to review the scientific literature about novel head and neck cancer diagnostics - epigenetic biomarkers. EVIDENCE ACQUISITION: A comprehensive review of the current literature was conducted according to the PRISMA guidelines by accessing the NCBI PubMed database. Authors conducted the search of articles in English language published from 2004 to 2015. EVIDENCE SYNTHESIS: A total of thirty three relevant studies were included in the review. …Fifteen of them concerned DNA methylation alterations, nine evaluation of abundancies in histone expressions and nine miRNA expression changes in HNC. CONCLUSIONS: Considerable number of epigenetic biomarkers have been identified in both tumor tissue and salivary samples. Genes with best diagnostic effectiveness rates and further studying prospects were: TIMP3, DCC, DAPK, CDH1, CCNA1, AIM1, MGMT, HIC1, PAX1, PAX5, ZIC4, p16, EDNRB, KIF1A, MINT31, CD44, RARβ , ECAD. Individual histone and miRNA alterations tend to be hnc specific. Prognostic values of separate biomarkers are ambiguous. No established standards for molecular assay of head and neck cancer was found in order to elude the paradoxical results and discrepancies in separate trials. Show more
Keywords: Head and neck cancer, DNA methylation, head and neck cancer histone, head and neck cancer miRNA
DOI: 10.3233/CBM-160666
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 487-502, 2016
Article Type: Other
Citation: Cancer Biomarkers, vol. 17, no. 4, pp. 503-509, 2016
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