Rong Yuhan, Kato Ikuma, Okubo Naoki, Tsuyuki Sho, Katsuta Eriko, Kobayashi Noritoshi, Nakagawa Kazuya, Ozawa Mayumi, Watanabe Jun, Ishibe Atsushi, Yamanaka Shoji, Fujii Satoshi, Endo Itaru, Ichikawa Yasushi
Department of Oncology, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa 236-0004, Japan.
Department of Molecular Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa 236-0004, Japan.
Mol Clin Oncol. 2024 Oct 3;21(6):91. doi: 10.3892/mco.2024.2789. eCollection 2024 Dec.
Neuroendocrine carcinoma (NEC) of the colon and rectum is a rare malignancy with a poor prognosis that is characterized by distinct clinical and histopathological features that differ significantly from those of more prevalent adenocarcinomas. Poorly differentiated colorectal adenocarcinoma (PDC) is also rare and carries a poor prognosis. Considering the morphological similarities between these two rare, poorly differentiated cancers of the colon and rectum, it is plausible that certain cases of colorectal cancer (CRC) diagnosed as PDC may contain NEC as well. In the present study, cases of CRC that were diagnosed as PDC at our institution were investigated, searching for patients who exhibited NEC characteristics based on the expression of neuroendocrine markers (NEMs), including chromogranin A, synaptophysin and insulinoma-associated 1 (INSM1), and the loss of retinoblastoma 1 (Rb). Of 816 total CRC cases, 74 cases (9.1%) were identified as PDC. These were further divided into 13 (17.5%) cases that were positive for NEMs and others. Of these 13 cases, the expression rates for chromogranin A and synaptophysin were 69.2% each, while that of INSM1 was 100%. Upon re-examination of the 13 PDC cases, two cases were morphologically identified as NEC, including one large- and one small-cell NEC. A total of two cases showed loss of Rb in their PDC lesions. NEM positivity was considered an independent prognostic factor in the 74 PDC cases. Among these cases, some may exhibit characteristics of NEC. Unraveling the molecular mechanisms using CRC that harbors both PDC and NEC will be a task for future research.
结肠和直肠神经内分泌癌(NEC)是一种罕见的恶性肿瘤,预后较差,具有独特的临床和组织病理学特征,与更常见的腺癌有显著差异。低分化结直肠癌(PDC)也很罕见,预后不良。考虑到这两种罕见的结肠和直肠低分化癌在形态学上的相似性,一些被诊断为PDC的结直肠癌(CRC)病例可能也包含NEC。在本研究中,对在我们机构被诊断为PDC的CRC病例进行了调查,寻找基于神经内分泌标志物(NEMs)表达表现出NEC特征的患者,这些标志物包括嗜铬粒蛋白A、突触素和胰岛素瘤相关蛋白1(INSM1),以及视网膜母细胞瘤1(Rb)的缺失。在总共816例CRC病例中,74例(9.1%)被确定为PDC。这些病例进一步分为13例(17.5%)NEMs阳性病例和其他病例。在这13例病例中,嗜铬粒蛋白A和突触素的表达率均为69.2%,而INSM1的表达率为100%。在对这13例PDC病例进行重新检查时,有2例在形态学上被鉴定为NEC,包括1例大细胞NEC和1例小细胞NEC。共有2例在其PDC病变中显示Rb缺失。在74例PDC病例中,NEMs阳性被认为是一个独立的预后因素。在这些病例中,一些可能表现出NEC的特征。利用同时具有PDC和NEC的CRC来阐明分子机制将是未来研究的一项任务。