Literature DB >> 23825028

Meta-analysis of transcriptome reveals let-7b as an unfavorable prognostic biomarker and predicts molecular and clinical subclasses in high-grade serous ovarian carcinoma.

Zhiqun Tang1, Ghim Siong Ow, Jean Paul Thiery, Anna V Ivshina, Vladimir A Kuznetsov.   

Abstract

High-grade serous ovarian carcinoma (HG-SOC) is a heterogeneous, poorly classified, lethal disease that frequently exhibits altered expressions of microRNAs. Let-7 family members are often reported as tumor suppressors; nonetheless, clinicopathological functions and prognostic values of individual let-7 family members have not been addressed in HG-SOC. In our work, we performed an integrative study to investigate the potential roles, clinicopathological functions and prognostic values of let-7 miRNA family in HG-SOC. Using microarray and clinical data of 1,170 HG-SOC patients, we developed novel survival prediction and system biology methods to analyze prognostic values and functional associations of let-7 miRNAs with global transcriptome and clinicopathological factors. We demonstrated that individual let-7 members exhibit diverse evolutionary history and distinct regulatory characteristics. Statistical tests and network analysis suggest that let-7b could act as a global synergistic interactor and master regulator controlling hundreds of protein-coding genes. The elevated expression of let-7b is associated with poor survival rates, which suggests an unfavorable role of let-7b in treatment response for HG-SOC patients. A novel let-7b-defined 36-gene prognostic survival signature outperforms many clinicopathological parameters, and stratifies HG-SOC patients into three high-confidence, reproducible, clinical subclasses: low-, intermediate- and high-risk, with 5-year overall survival rates of 56-71%, 12-29% and 0-10%, respectively. Furthermore, the high-risk and low-risk subclasses exhibit strong mesenchymal and proliferative tumor phenotypes concordant with resistance and sensitivity to primary chemotherapy. Our results have led to identification of promising prognostic markers of HG-SOC, which could provide a rationale for genetic-based stratification of patients and optimization of treatment regimes.
© 2013 UICC.

Entities:  

Keywords:  cancer biomarker; high-grade serous ovarian carcinoma; microRNA let-7; survival prognosis; tumor classification

Mesh:

Substances:

Year:  2013        PMID: 23825028     DOI: 10.1002/ijc.28371

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  32 in total

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2.  Expression of serum let-7c, let-7i, and let-7f microRNA with its target gene, pepsinogen C, in gastric cancer and precancerous disease.

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3.  Regulation of tumor cell migration and invasion by the H19/let-7 axis is antagonized by metformin-induced DNA methylation.

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Journal:  Oncogene       Date:  2014-08-04       Impact factor: 9.867

4.  MicroRNA-613 inhibited ovarian cancer cell proliferation and invasion by regulating KRAS.

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Journal:  Tumour Biol       Date:  2015-12-02

5.  A ranking-based meta-analysis reveals let-7 family as a meta-signature for grade classification in breast cancer.

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Review 6.  MicroRNAs: New Biomarkers for Diagnosis, Prognosis, Therapy Prediction and Therapeutic Tools for Breast Cancer.

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7.  Multiple signatures of a disease in potential biomarker space: Getting the signatures consensus and identification of novel biomarkers.

Authors:  Ghim Siong Ow; Vladimir A Kuznetsov
Journal:  BMC Genomics       Date:  2015-06-11       Impact factor: 3.969

Review 8.  Impact of Nutrition on Non-Coding RNA Epigenetics in Breast and Gynecological Cancer.

Authors:  Rosanna H E Krakowsky; Trygve O Tollefsbol
Journal:  Front Nutr       Date:  2015-05-27

Review 9.  Getting to know ovarian cancer ascites: opportunities for targeted therapy-based translational research.

Authors:  Nuzhat Ahmed; Kaye L Stenvers
Journal:  Front Oncol       Date:  2013-09-25       Impact factor: 6.244

10.  Identification of two poorly prognosed ovarian carcinoma subtypes associated with CHEK2 germ-line mutation and non-CHEK2 somatic mutation gene signatures.

Authors:  Ghim Siong Ow; Anna V Ivshina; Gloria Fuentes; Vladimir A Kuznetsov
Journal:  Cell Cycle       Date:  2014-05-30       Impact factor: 4.534

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