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A Comprehensive Analysis of Somatic Alterations in Chinese Ovarian Cancer Patients

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Journal Sci Rep
Specialty Science
Date 2021 Jan 12
PMID 33432021
Citations 10
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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.

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References
1.
Jayson G, Kohn E, Kitchener H, Ledermann J . Ovarian cancer. Lancet. 2014; 384(9951):1376-88. DOI: 10.1016/S0140-6736(13)62146-7. View

2.
. Integrated genomic analyses of ovarian carcinoma. Nature. 2011; 474(7353):609-15. PMC: 3163504. DOI: 10.1038/nature10166. View

3.
Jorge S, Swisher E, Norquist B, Pennington K, Gray H, Urban R . Patterns and duration of primary and recurrent treatment in ovarian cancer patients with germline mutations. Gynecol Oncol Rep. 2019; 29:113-117. PMC: 6710556. DOI: 10.1016/j.gore.2019.08.001. View

4.
Blanco I, Kuchenbaecker K, Cuadras D, Wang X, Barrowdale D, Ruiz de Garibay G . Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers. PLoS One. 2015; 10(4):e0120020. PMC: 4382299. DOI: 10.1371/journal.pone.0120020. View

5.
Monk B, Coleman R . Changing the paradigm in the treatment of platinum-sensitive recurrent ovarian cancer: from platinum doublets to nonplatinum doublets and adding antiangiogenesis compounds. Int J Gynecol Cancer. 2009; 19 Suppl 2:S63-7. DOI: 10.1111/IGC.0b013e3181c104fa. View