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      KCI등재 SCOPUS SCIE

      Genomic mutation profiling using liquid biopsy in Korean patients with prostate cancer: Circulating tumor DNA mutation predicts the development of castration resistance

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      https://www.riss.kr/link?id=A107299994

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      다국어 초록 (Multilingual Abstract)

      Purpose: To investigate germline and somatic mutation profiles in Korean patients with prostate cancer using liquid biopsy and solid tissue testing and to evaluate the prognostic value of circulating tumor DNA (ctDNA) in predicting castration resistan...

      Purpose: To investigate germline and somatic mutation profiles in Korean patients with prostate cancer using liquid biopsy and solid tissue testing and to evaluate the prognostic value of circulating tumor DNA (ctDNA) in predicting castration resistance in patients with metastatic hormone-sensitive prostate cancer (mHSPC).
      Materials and Methods: Plasma samples from 56 prostate cancer patients were subjected to next-generation sequencing (NGS) to identify germline mutations and ctDNA analysis using liquid biopsy to detect somatic mutations. Additionally, paired solid cancer tissues from 18 patients were subject to NGS to detect somatic mutations. The clinical parameters and ctDNA profiles of patients with mHSPC were analyzed to evaluate the prognostic value of ctDNA mutations with respect to predicting castration resistance using Cox proportional hazards regression analysis.
      Results: Germline mutations occurred in 3.6% of the patients in this cohort, with mutations identified in RAD50 (1.8%) and BRCA1 (1.8%). Somatic mutations detected by liquid biopsy and solid tissue testing were common in TP53 (12.5%), PIK3CA (3.6%), and TMPRSS2-ERG (3.6%). Of the 18 patients with paired tissue testing, two patients had at least one identical somatic mutation in both the liquid biopsy and solid tissue testing. In patients with mHSPC, the presence of ctDNA mutations could independently predict the castration resistance development (hazard ratio, 13.048; 95% confidential interval, 1.109–153.505; p=0.041).
      Conclusions: Korean patients with prostate cancer showed a relatively low germline mutation rate compared to other ethnicities. The ctDNA mutations detected by liquid biopsy can predict the development of castration resistance in patients with mHSPC.

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      참고문헌 (Reference)

      1 Cancer Genome Atlas Research Network, "The molecular taxonomy of primary prostate cancer" 163 : 1011-1025, 2015

      2 Nicolosi P, "Prevalence of germline variants in prostate cancer and implications for current genetic testing guidelines" 5 : 523-528, 2019

      3 Liu Z, "Presence of allele frequency heterogeneity defined by ctDNA profiling predicts unfavorable overall survival of NSCLC" 8 : 1045-1050, 2019

      4 Benafif S, "PRACTICAL Consortium. A review of prostate cancer genome-wide association studies (GWAS)" 27 : 845-857, 2018

      5 Todd M. Morgan, "Liquid biopsy: Where did it come from, what is it, and where is it going?" 대한비뇨의학회 60 (60): 139-141, 2019

      6 Pritchard CC, "Inherited DNA-repair gene mutations in men with metastatic prostate cancer" 375 : 443-453, 2016

      7 강민용, "Genomic analysis of Korean patients with advanced prostate cancer by use of a comprehensive next-generation sequencing panel and low-coverage, whole-genome sequencing" 대한비뇨의학회 60 (60): 227-234, 2019

      8 Lambert AW, "Emerging biological principles of metastasis" 168 : 670-691, 2017

      9 Klein EA, "Development of a comprehensive cell-free DNA (cfDNA) assay for early detection of multiple tumor types: the Circulating Cell-free Genome Atlas (CCGA) study" 36 (36): 12021-, 2018

      10 Scher HI, "Design and end points of clinical trials for patients with progressive prostate cancer and castrate levels of testosterone : recommendations of the Prostate Cancer Clinical Trials Working Group" 26 : 1148-1159, 2008

      1 Cancer Genome Atlas Research Network, "The molecular taxonomy of primary prostate cancer" 163 : 1011-1025, 2015

      2 Nicolosi P, "Prevalence of germline variants in prostate cancer and implications for current genetic testing guidelines" 5 : 523-528, 2019

      3 Liu Z, "Presence of allele frequency heterogeneity defined by ctDNA profiling predicts unfavorable overall survival of NSCLC" 8 : 1045-1050, 2019

      4 Benafif S, "PRACTICAL Consortium. A review of prostate cancer genome-wide association studies (GWAS)" 27 : 845-857, 2018

      5 Todd M. Morgan, "Liquid biopsy: Where did it come from, what is it, and where is it going?" 대한비뇨의학회 60 (60): 139-141, 2019

      6 Pritchard CC, "Inherited DNA-repair gene mutations in men with metastatic prostate cancer" 375 : 443-453, 2016

      7 강민용, "Genomic analysis of Korean patients with advanced prostate cancer by use of a comprehensive next-generation sequencing panel and low-coverage, whole-genome sequencing" 대한비뇨의학회 60 (60): 227-234, 2019

      8 Lambert AW, "Emerging biological principles of metastasis" 168 : 670-691, 2017

      9 Klein EA, "Development of a comprehensive cell-free DNA (cfDNA) assay for early detection of multiple tumor types: the Circulating Cell-free Genome Atlas (CCGA) study" 36 (36): 12021-, 2018

      10 Scher HI, "Design and end points of clinical trials for patients with progressive prostate cancer and castrate levels of testosterone : recommendations of the Prostate Cancer Clinical Trials Working Group" 26 : 1148-1159, 2008

      11 Wyatt AW, "Concordance of circulating tumor DNA and matched metastatic tissue biopsy in prostate cancer" 109 : djx118-, 2017

      12 Lorente D, "Circulating tumour cell increase as a biomarker of disease progression in metastatic castration-resistant prostate cancer patients with low baseline CTC counts" 29 : 1554-1560, 2018

      13 de Bono JS, "Circulating tumor cells predict survival benefit from treatment in metastatic castration-resistant prostate cancer" 14 : 6302-6309, 2008

      14 Goldkorn A, "Circulating tumor cell telomerase activity as a prognostic marker for overall survival in SWOG 0421 : a phase III metastatic castration resistant prostate cancer trial" 136 : 1856-1862, 2015

      15 Heller G, "Circulating tumor cell number as a response measure of prolonged survival for metastatic castrationresistant prostate cancer : a comparison with prostate-specific antigen across five randomized phase III clinical trials" 36 : 572-580, 2018

      16 Annala M, "Circulating tumor DNA genomics correlate with resistance to abiraterone and enzalutamide in prostate cancer" 8 : 444-457, 2018

      17 Sweeney CJ, "Chemohormonal therapy in metastatic hormone-sensitive prostate cancer" 373 : 737-746, 2015

      18 Schumacher FR, "Association analyses of more than 140, 000 men identify 63 new prostate cancer susceptibility loci" 50 : 928-936, 2018

      19 AACR Project GENIE Consortium, "AACR Project GENIE : powering precision medicine through an international consortium" 7 : 818-831, 2017

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2019-03-12 학회명변경 한글명 : 대한비뇨기과학회 -> 대한비뇨의학회 KCI등재
      2016-03-04 학술지명변경 외국어명 : 미등록 -> Investigative and Clinical Urology KCI등재
      2016-01-15 학술지명변경 한글명 : Korean Journal of Urology -> Investigative and Clinical Urology KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-02-21 학술지명변경 한글명 : 대한비뇨기과학회지 -> Korean Journal of Urology
      외국어명 : The Korean Journal of Urology -> 미등록
      KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.14 0.14 0.13
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.12 0.314 0.23
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