肠型极好分化胃腺癌的基因组和病理图谱分析:以扩散型转化为重点的研究。

Hirofumi Rokutan, Yasuhito Arai, Akiko Kunita, Satoshi Yamasaki, Hiromi Nakamura, Natsuko Hama, Atsuhito Nakayama, Fumie Hosoda, Yasushi Totoki, Mitsuhiro Fujishiro, Yasuyuki Seto, Tatsuhiro Shibata, Tetsuo Ushiku
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摘要

肠型分化很好的腺癌是胃癌的一个独特亚型,其特点是吻合腺体呈手拉手状,细胞学不典型性低,类似肠化生。这种肿瘤生长缓慢,临床症状不明显,但也有一部分会转变为组织学分级较高的腺癌,典型的是弥漫型癌,表现为侵袭性。本研究旨在更好地描述其基因组和病理特征,重点关注与弥漫型转化相关的因素。研究人员对58例弥漫型转化(31例)和非弥漫型转化(27例)病例的分子和病理特征进行了分析。首先,对18个病例(发现队列)进行了全面的深度DNA测序,然后对40个病例(验证队列)的热点RHOA突变进行了数字液滴聚合酶链反应。总的来说,RHOA突变是最常见的改变(34%),其次是ARID1A缺失(12%)、p53改变(10%)和CLDN18::ARHGAP26/6融合(3.4%)。在一个伴有 p53 改变的晚期病例中发现了 FGFR2 扩增。p53表达的改变仅在高分级成分中被发现,并与晚期疾病(P=0.0015)和弥漫型转化(P=0.026)显著相关。混合粘蛋白表型也与晚期疾病(P<0.001)和弥散型转化(P<0.001)密切相关。在内聚力差的成分中经常观察到 E-cadherin 表达减少(74%)。这项研究表明,RHOA 突变弥漫型胃癌的一部分是由分化非常好的肠型腺癌转化而来的。我们的观察结果表明,混合粘蛋白表型是一种风险因素,p53和E-cadherin的改变是弥散型转化的驱动因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic and Pathologic Profiling of Very Well-Differentiated Gastric Adenocarcinoma of Intestinal Type: A Study With Emphasis on Diffuse-Type Transformation.
Very well-differentiated adenocarcinoma of intestinal type is a distinct subtype of gastric cancer characterized by anastomosing glands with a hand-in-hand pattern and low-grade cytologic atypia resembling intestinal metaplasia. This is a slow-growing neoplasm with an indolent clinical course; however, a subset demonstrates transformation into adenocarcinoma with higher-grade histology, typically diffuse-type carcinoma, and behaves aggressively. This study aimed to better characterize the genomic and pathologic features, with a focus on factors associated with diffuse-type transformation. A total of 58 cases with (n=31) and without (n=27) diffuse-type transformation were analyzed for molecular and pathologic features. First, comprehensive deep DNA sequencing was conducted in 18 cases (discovery cohort), followed by a digital droplet polymerase chain reaction of hot spot RHOA mutations in 40 cases (validation cohort). In total, RHOA mutations were the most common alteration (34%), followed by loss of ARID1A (12%), p53 alterations (10%), and CLDN18::ARHGAP26/6 fusions (3.4%). FGFR2 amplification was identified in an advanced case with a p53 alteration. Altered p53 expression was recognized only in higher-grade components and was significantly associated with advanced disease (P=0.0015) and diffuse-type transformation (P=0.026). A mixed mucin phenotype was also strongly correlated with advanced disease (P<0.001) and diffuse-type transformation (P<0.001). Decreased E-cadherin expression was frequently observed (74%) in poorly cohesive components. This study demonstrated that a subset of RHOA-mutant diffuse-type gastric cancers develops through the transformation of very well-differentiated adenocarcinoma of intestinal type. Our observations suggest a mixed mucin phenotype as a risk factor and alterations in p53 and E-cadherin as drivers of diffuse-type transformation.
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