Molecular Analysis of the KIT Gene in Gastrointestinal Stromal Tumors With Novel Mutations

被引:7
|
作者
Calibasi, Gizem [1 ]
Baskin, Yasemin [1 ]
Alyuruk, Hakan [2 ]
Cavas, Levent [3 ]
Oztop, Ilhan [4 ]
Sagol, Ozgul [5 ]
Atila, Koray [6 ]
Ellidokuz, Hulya [7 ]
Yilmaz, Ugur [4 ]
机构
[1] Dokuz Eylul Univ, Dept Basic Oncol, Inst Oncol, TR-35350 Izmir, Turkey
[2] Grad Sch Nat & Appl Sci, Izmir, Turkey
[3] Fac Sci, Dept Chem, Div Biochem, Izmir, Turkey
[4] Fac Med, Dept Med Oncol, Izmir, Turkey
[5] Fac Med, Dept Pathol, Izmir, Turkey
[6] Fac Med, Dept Surg, Izmir, Turkey
[7] Inst Oncol, Dept Prevent Oncol, Izmir, Turkey
关键词
gastrointestinal stromal tumors; KIT gene; pharmacogenomics; DNA sequencing; bioinformatics; C-KIT; KINASE MUTATIONS; IMATINIB; PROGNOSIS; RECEPTOR; GISTS; ASSOCIATION; SUNITINIB; PDGFRA; DOMAIN;
D O I
10.1097/PAI.0b013e318284a074
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. KIT gene mutations have great importance for GISTs. This study evaluated the relationship between KIT mutations and GIST clinicopathologic features to define region-specific and population-specific differences. Genomic DNA was extracted from 60 GISTs, and polymerase chain reaction was performed for KIT gene exons 9, 11, 13, and 17. Polymerase chain reaction amplicons were sequenced in both directions. This study represents the first mutation data of the KIT gene in GISTs from a Turkish population and reports novel mutations. The mutation rate in exon 11 (46.7%) was remarkably higher than those of the other exons (8.3% for exon 9; 11.7% for exon 13; 1.7% for exon 17). There was an association between malignancy potential and the presence of KIT mutations (odds ratio=3.18). Cases with mutations in codons W557-K558 in exon 11 had 11-fold greater risk of malignancy when compared with those without a mutation in this exon (odds ratio=11). We report different mutations than those previously reported, which emphasizes the importance of personalized medicine that could be empowered by the use of bioinformatics tools in the diagnostic process and therapeutic approaches.
引用
收藏
页码:37 / 45
页数:9
相关论文
共 50 条
  • [1] Analysis of C-KIT mutations in gastrointestinal stromal tumors
    Beliakov, I.
    Mazurenko, N.
    Anurova, O.
    Snigur, P.
    Selchuk, V.
    EJC SUPPLEMENTS, 2005, 3 (02): : 216 - 216
  • [2] Spectrum of KIT gene mutations in Korean patients with gastrointestinal stromal tumors
    Jung, S.
    Lee, K.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 424 - 424
  • [3] KIT gene mutations in gastrointestinal stromal tumor
    Kang, Weiming
    Zhu, Changzhen
    Yu, JianChun
    Ye, Xin
    Ma, ZhiQiang
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2015, 20 : 919 - 926
  • [4] Clinicopathological and Molecular Characterization of KIT and PDGFRA Mutations in Advanced Gastrointestinal Stromal Tumors
    Alsuwaidan, A.
    Verma, U.
    Gopal, P.
    Hwang, H.
    Wachsmann, M.
    Oliver, D.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2018, 20 (06): : 998 - 998
  • [5] Frequent KIT Mutations in Human Gastrointestinal Stromal Tumors
    Xu, Zhi
    Huo, Xinying
    Tang, Chuanning
    Ye, Hua
    Nandakumar, Vijayalakshmi
    Lou, Feng
    Zhang, Dandan
    Jiang, Shouwen
    Sun, Hong
    Dong, Haichao
    Zhang, Guangchun
    Liu, Zhiyuan
    Dong, Zhishou
    Guo, Baishuai
    Yan, He
    Yan, Chaowei
    Wang, Lu
    Su, Ziyi
    Li, Yangyang
    Gu, Dongying
    Zhang, Xiaojing
    Wu, Xiaomin
    Wei, Xiaowei
    Hong, Lingzhi
    Zhang, Yangmei
    Yang, Jinsong
    Gong, Yonglin
    Tang, Cuiju
    Jones, Lindsey
    Huang, Xue F.
    Chen, Si-Yi
    Chen, Jinfei
    SCIENTIFIC REPORTS, 2014, 4
  • [6] KIT and PDGFRA mutations in gastrointestinal stromal tumors (GISTs)
    Lasota, Jerzy
    Miettinen, Markku
    SEMINARS IN DIAGNOSTIC PATHOLOGY, 2006, 23 (02) : 91 - 102
  • [7] Frequent KIT Mutations in Human Gastrointestinal Stromal Tumors
    Zhi Xu
    Xinying Huo
    Chuanning Tang
    Hua Ye
    Vijayalakshmi Nandakumar
    Feng Lou
    Dandan Zhang
    Shouwen Jiang
    Hong Sun
    Haichao Dong
    Guangchun Zhang
    Zhiyuan Liu
    Zhishou Dong
    Baishuai Guo
    He Yan
    Chaowei Yan
    Lu Wang
    Ziyi Su
    Yangyang Li
    Dongying Gu
    Xiaojing Zhang
    Xiaomin Wu
    Xiaowei Wei
    Lingzhi Hong
    Yangmei Zhang
    Jinsong Yang
    Yonglin Gong
    Cuiju Tang
    Lindsey Jones
    Xue F. Huang
    Si-Yi Chen
    Jinfei Chen
    Scientific Reports, 4
  • [8] Biology of gastrointestinal stromal tumors:: KIT mutations and beyond
    Duensing, A
    Heinrich, MC
    Fletcher, CDM
    Fletcher, JA
    CANCER INVESTIGATION, 2004, 22 (01) : 106 - 116
  • [9] C-KIT MUTATIONS IN GASTROINTESTINAL STROMAL TUMORS
    La Paglia, L.
    Badalamenti, G.
    Amodeo, V.
    Bruno, L.
    Calo, V.
    Corsini, L. R.
    D'Andrea, A.
    Fanale, D.
    Insalaco, L.
    Margarese, N.
    Terrasi, M.
    Napoli, L.
    Damiani, G. B.
    Di Piazza, F.
    Miraglia, M. C.
    Bazan, V.
    Russo, A.
    CANCER TREATMENT REVIEWS, 2010, 36 : S96 - S96
  • [10] KIT and PDGFRA Mutations in Gastrointestinal Stromal Tumors in India
    Shetty, O.
    Pai, T.
    Gurav, M.
    Bal, M.
    Ramadwar, M.
    Arora, I.
    Kurani, H.
    Rumde, R.
    Dhanavade, D.
    Ostwal, V.
    Desai, S.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2015, 17 (06): : 826 - 827