Literature DB >> 27939411

Identification of novel mutations in Japanese ovarian clear cell carcinoma patients using optimized targeted NGS for clinical diagnosis.

Yoshiaki Maru1, Naotake Tanaka2, Miki Ohira3, Makiko Itami4, Yoshitaka Hippo5, Hiroki Nagase6.   

Abstract

OBJECTIVE: Ovarian clear cell carcinoma (OCCC) is an aggressive ovarian cancer with a higher frequency in Japan and often becomes chemorefractory disease. Reliable genetic diagnosis is essential to affirm the success of precision medicine for OCCC treatment. The aim of this study is, therefore, to identify novel mutations in OCCCs and develop a feasible clinical next generation sequencing (NGS) approach using formalin-fixed paraffin-embedded (FFPE) rather than preferable but not always available fresh frozen (FF) samples.
METHODS: We optimized and evaluated exome analyses of 409 cancer-related genes using FFPE and FF DNA and analyzed NGS data to identify somatic mutations in Japanese OCCCs.
RESULTS: Sufficient and good quality DNAs from FFPE samples were extracted from 18 (FIGO Stage I: 12) out of 29 pairs of matched normal and OCCC for NGS (63%). The fine quality of extracted DNAs depended on the length of storage period (<2years storage). We also identified 45 somatic mutations in 34 genes including unreported variants from those FFPE DNA, in which somatic mutations in the PIK3CA gene was the most common (28%) as previously reported. Seven genes (PIK3CA, ARID1A, CTNNB1, CSMD3, LPHN3, LRP1B, and TP53) were mutated in at least two independent OCCCs. FF samples from 3 out of those 18 OCCCs were available and 13 out of 14 FFPE somatic mutations were confirmed.
CONCLUSIONS: We successfully identified novel genetic alterations in Japanese OCCCs and demonstrated a feasible clinical diagnostic procedure using targeted NGS for OCCC FFPE samples.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Clinical sequencing; FFPE; Next-generation sequencing; Ovarian clear cell carcinoma; Somatic mutations

Mesh:

Year:  2016        PMID: 27939411     DOI: 10.1016/j.ygyno.2016.11.045

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  19 in total

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5.  Loss and gain of N-linked glycosylation sequons due to single-nucleotide variation in cancer.

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8.  Establishment and characterization of patient-derived organoids from a young patient with cervical clear cell carcinoma.

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Review 9.  Current Status of Patient-Derived Ovarian Cancer Models.

Authors:  Yoshiaki Maru; Yoshitaka Hippo
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Review 10.  Genomic alterations in gynecological malignancies: histotype-associated driver mutations, molecular subtyping schemes, and tumorigenic mechanisms.

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Journal:  J Hum Genet       Date:  2021-06-07       Impact factor: 3.172

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