4.3 Article

The genetic difference between Western and Chinese urothelial cell carcinomas: infrequent FGFR3 mutation in Han Chinese patients

Journal

ONCOTARGET
Volume 7, Issue 18, Pages 25826-25835

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.8404

Keywords

FGFR3 mutation; racial disparity; TERT promoter mutation; urothelial bladder carcinoma; upper track urothelial carcinoma

Funding

  1. National Basic Research Program of China [2012CB911202]
  2. Adolf H. Lundin Charitable Foundation
  3. Swedish Cancer Society
  4. Swedish Research Council
  5. Cancer Society in Stockholm
  6. National Natural Science Foundation of China [81572515, 81472395, 81372765, 81502409]
  7. Shandong Provincial Natural Science Foundation, China [ZR2011HM055, ZR2014HQ035]

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Urothelial cell carcinoma (UCC) includes urothelial bladder carcinoma (UBC), renal pelvic carcinoma (RPC) and ureter carcinoma (UC), and its incidence varies dependent on geographical areas and tumor locations, which indicates different oncogenic mechanisms and/or different genetic susceptibility/environment exposure. The activating mutations of the fibroblast growth factor receptor 3 (FGFR3) gene and telomerase reverse transcriptase (TERT) promoter are the most frequent genetic events in UCCs. These mutations have clinical utilities in UCC initial diagnostics, prognosis, recurrence monitoring and management. However, the vast majority of the results are obtained from studies of UCC patients in Western countries, and little has been known about these in Han Chinese patients. In the present study, we screened the FGFR3 gene and TERT promoter for mutations in 116 UBC, 91 RPC and 115 UC tumors from Han Chinese patients by using Sanger Sequencing. TERT promoter mutations occurred at a high frequency in these UCC patients, comparable with that seen in Western patients, however, the FGFR3 mutation was surprisingly lower, only 9.4% for UBCs, 8.8% for RPCs and 2.6% for UCs, respectively. Taken together, the FGFR3 gene is an infrequent target in the pathogenesis of Han Chinese UCCs, and its mutation detection and targeted therapy have limited clinical utility in these patients. Our results underscore the need for extensive characterization of cancer genomes from diverse patient populations, thereby contributing to precision medicine for cancer treatment and prevention.

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