Germline DNA-Repair Genes and HOXB13 Mutations in Korean Men with Metastatic Prostate Cancer: Data from a Large Korean Cohort

被引:3
|
作者
Song, Sang Hun [1 ,2 ]
Kim, Hak-Min [3 ]
Jung, Yu Jin [4 ]
Kook, Ha Rim [2 ,5 ]
Jeon, Sungwon [6 ,7 ]
Bhak, Jong [6 ,7 ,8 ,9 ]
Kim, Jin Hyuck [1 ,2 ]
Lee, Hakmin [1 ,2 ]
Oh, Jong Jin [1 ,2 ]
Lee, Sangchul [1 ,2 ]
Hong, Sung Kyu [1 ,2 ]
Byun, Seok-Soo [1 ,3 ,4 ,10 ]
机构
[1] Seoul Natl Univ, Bundang Hosp, Dept Urol, Seongnam, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Urol, Seoul, South Korea
[3] Procagen, Seongnam, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Med Device Dev, Seoul, South Korea
[5] Seoul N Urol Clin, Seongnam, South Korea
[6] Ulsan Natl Inst Sci & Technol, Korean Genom Ctr, Ulsan, South Korea
[7] Clinomics Inc, Ulsan, South Korea
[8] Ulsan Natl Inst Sci & Technol, Coll Informat Bio Convergence Engn, Dept Biomed Engn, Ulsan, South Korea
[9] Genome Res Fdn, Personal Genom Inst, Osong, South Korea
[10] Seoul Natl Univ, Bundang Hosp, Dept Urol, 82 Gumi Ro 173Beon Gil, Seongnam 13620, South Korea
关键词
Asians; Prostatic neoplasms; DNA damage; Genetics; RISK; VARIANTS; NUMBER; GENOME;
D O I
10.5534/wjmh.220190
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Purpose: Germline mutations in DNA damage repair (DDR) genes such as BRCA2 have been associated with prostate cancer (PC) risk but has not been thoroughly evaluated for metastatic prostate cancer (mPC) in Asian men. This study attempts to evaluate frequency of DDR mutations in the largest cohort of Koreans. Materials and Methods: We recruited 340 patients with mPC unselected for family history of cancer and compared to 495 controls. Whole genome sequencing was applied to assess germline pathogenic/likely pathogenic variants (PV/LPVs) in 26 DDR genes and HOXB13, including 7 genes (ATM, BRCA1/2, CHEK2, BRIP1, PALB2, and NBN) associated with hereditary PC. Comparisons to published Caucasian and Japanese cohorts were performed. Results: Total of 28 PV/LPVs were identified in 30 (8.8%) patients; mutations were found in 13 genes, including BRCA2 (15 men [4.41%]), ATM (2 men [0.59%]), NBN (2 men [0.59%], and BRIP1 (2 men [0.59%]). Only one patient had HOXB13 mutation (0.29%). A lower rate of overall germline variant frequency was observed in Korean mPC compared to Caucasians (8.8% vs. 11.8%), but individual variants notably differed from Caucasian and geographically similar Japanese cohorts. PV/ LPVs in DDR genes tended to increase gradually with higher Gleason scores (GS 7, 7.1%; GS 8, 7.5%; GS 9-10, 9.9%).Conclusions: BRCA2 was the most frequently mutated gene common to different cohorts supporting its importance, but dif-ferences in variant distribution in Korean mPC underscore the need for ethnic-specific genetic models. Future ethnic-specific analyses are warranted to verify our findings.
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页码:960 / 968
页数:9
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