Liu Cheng, McKeone Diane M, Walker Neal I, Bettington Mark L, Leggett Barbara A, Whitehall Vicki L J
The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
The School of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
Histopathology. 2017 Jun;70(7):1079-1088. doi: 10.1111/his.13180. Epub 2017 Mar 22.
Activating mutations in GNAS are important in the development of a range of neoplasms, including a small proportion of conventional adenomas and colorectal carcinomas (CRCs). However, their contribution to serrated pathway neoplasia is unclear, as mutations have only been examined in small series of sessile serrated adenomas (SSAs) and traditional serrated adenomas (TSAs), and not in serrated tubulovillous adenomas (sTVAs). The aim of this study was to investigate the frequency and significance of GNAS mutations in colorectal adenomas and CRCs.
Using a large, well-characterized series, we identified GNAS mutations in 9.2% (18 of 196) of TSAs, 7.1% (four of 56) of sTVAs and 2.0% (nine of 459) of CRCs. Mutations were absent in SSAs (none of 43), tubular adenomas (none of 50) and conventional tubulovillous adenomas (none of 50). A BRAF or KRAS mutation was seen in 77.4% of GNAS mutant lesions, suggesting a synergistic effect with the mitogen-activated protein kinase pathway. In CRCs, GNAS mutations were associated with mucinous differentiation and serrated morphological features.
GNAS mutations contribute significantly to the development of a subset of serrated adenomas and CRCs.
GNAS基因的激活突变在一系列肿瘤的发生发展中具有重要作用,包括一小部分传统腺瘤和结直肠癌(CRC)。然而,其在锯齿状途径肿瘤形成中的作用尚不清楚,因为仅在少数无蒂锯齿状腺瘤(SSA)和传统锯齿状腺瘤(TSA)中检测到突变,而未在锯齿状管状绒毛状腺瘤(sTVA)中检测。本研究的目的是调查结直肠腺瘤和CRC中GNAS突变的频率及意义。
通过一个大型、特征明确的队列,我们在9.2%(196例中的18例)的TSA、7.1%(56例中的4例)的sTVA和2.0%(459例中的9例)的CRC中鉴定出GNAS突变。SSA(43例中无)、管状腺瘤(50例中无)和传统管状绒毛状腺瘤(50例中无)中未发现突变。在77.4%的GNAS突变病变中可见BRAF或KRAS突变,提示与丝裂原活化蛋白激酶途径存在协同作用。在CRC中,GNAS突变与黏液分化和锯齿状形态特征相关。
GNAS突变对一部分锯齿状腺瘤和CRC的发生发展有显著贡献。