Literature DB >> 33432021

A comprehensive analysis of somatic alterations in Chinese ovarian cancer patients.

Yingli Zhang1,2,3, Xiaoliang Shi4, Jiejie Zhang1,2,3, Xi Chen1,2,3, Peng Zhang4, Angen Liu4, Tao Zhu5,6,7.   

Abstract

Ovarian cancer is one of the most common cancers in women and is often diagnosed as advanced stage because of the subtle symptoms of early ovarian cancer. To identify the somatic alterations and new biomarkers for the diagnosis and targeted therapy of Chinese ovarian cancer patients, a total of 65 Chinese ovarian cancer patients were enrolled for detection of genomic alterations. The most commonly mutated genes in ovarian cancers were TP53 (86.15%, 56/65), NF1 (13.85%, 9/65), NOTCH3 (10.77%, 7/65), and TERT (10.77%, 7/65). Statistical analysis showed that TP53 and LRP1B mutations were associated with the age of patients, KRAS, TP53, and PTEN mutations were significantly associated with tumor differentiation, and MED12, LRP2, PIK3R2, CCNE1, and LRP1B mutations were significantly associated with high tumor mutational burden. The mutation frequencies of LRP2 and NTRK3 in metastatic ovarian cancers were higher than those in primary tumors, but the difference was not significant (P = 0.072, for both). Molecular characteristics of three patients responding to olapanib supported that BRCA mutation and HRD related mutations is the target of olaparib in platinum sensitive patients. In conclusion we identified the somatic alterations and suggested a group of potential biomarkers for Chinese ovarian cancer patients. Our study provided a basis for further exploration of diagnosis and molecular targeted therapy for Chinese ovarian cancer patients.

Entities:  

Year:  2021        PMID: 33432021      PMCID: PMC7801677          DOI: 10.1038/s41598-020-79694-0

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  64 in total

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Journal:  Breast Cancer Res Treat       Date:  2020-08-10       Impact factor: 4.872

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Journal:  Nature       Date:  2011-06-29       Impact factor: 49.962

7.  Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers.

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8.  Novel risk models for early detection and screening of ovarian cancer.

Authors:  Matthew R Russell; Alfonsina D'Amato; Ciaren Graham; Emma J Crosbie; Aleksandra Gentry-Maharaj; Andy Ryan; Jatinderpal K Kalsi; Evangelia-Ourania Fourkala; Caroline Dive; Michael Walker; Anthony D Whetton; Usha Menon; Ian Jacobs; Robert L J Graham
Journal:  Oncotarget       Date:  2017-01-03

9.  Identification of Novel Somatic TP53 Mutations in Patients with High-Grade Serous Ovarian Cancer (HGSOC) Using Next-Generation Sequencing (NGS).

Authors:  Marica Garziera; Erika Cecchin; Vincenzo Canzonieri; Roberto Sorio; Giorgio Giorda; Simona Scalone; Elena De Mattia; Rossana Roncato; Sara Gagno; Elena Poletto; Loredana Romanato; Franca Sartor; Jerry Polesel; Giuseppe Toffoli
Journal:  Int J Mol Sci       Date:  2018-05-18       Impact factor: 5.923

10.  Patterns and duration of primary and recurrent treatment in ovarian cancer patients with germline BRCA mutations.

Authors:  Soledad Jorge; Elizabeth M Swisher; Barbara M Norquist; Kathryn P Pennington; Heidi J Gray; Renata R Urban; Rochelle L Garcia; Kemi M Doll
Journal:  Gynecol Oncol Rep       Date:  2019-08-09
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  2 in total

1.  Somatic Mutational Profile of High-Grade Serous Ovarian Carcinoma and Triple-Negative Breast Carcinoma in Young and Elderly Patients: Similarities and Divergences.

Authors:  Pedro Adolpho de Menezes Pacheco Serio; Gláucia Fernanda de Lima Pereira; Maria Lucia Hirata Katayama; Rosimeire Aparecida Roela; Simone Maistro; Maria Aparecida Azevedo Koike Folgueira
Journal:  Cells       Date:  2021-12-20       Impact factor: 6.600

Review 2.  The role of mediator subunit 12 in tumorigenesis and cancer therapeutics.

Authors:  Cristian G Gonzalez; Shivani Akula; Marieke Burleson
Journal:  Oncol Lett       Date:  2022-01-10       Impact factor: 2.967

  2 in total

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