LGR5型
异位表达
病理
发育不良
干细胞
生物
干细胞标记物
潘尼斯电池
增生性息肉
祖细胞
癌症研究
结直肠癌
医学
癌症干细胞
癌症
细胞培养
结肠镜检查
小肠
细胞生物学
遗传学
生物化学
作者
Bo Gun Jang,Hye Sung Kim,Kyung Ju Kim,Ye‐Young Rhee,Woo Ho Kim,Gyeong Hoon Kang
摘要
Aims Intestinal stem cell ( ISC ) markers such as LGR 5 , ASCL 2 , EPHB 2 and OLFM 4 , and their clinical implications have been studied extensively in colorectal cancers ( CRC s). However, little is known about their expression in precancerous lesions of CRC s. Here, we investigated the expression and distribution of ISC markers in serrated polyps and conventional adenomas. Methods and results Reverse transcription–polymerase chain reaction ( RT – PCR ) analysis revealed that all ISC markers were up‐regulated significantly in conventional adenomas with low‐grade dysplasia ( CALG s) compared with other lesions. RNA in‐situ hybridization confirmed that CALG s exhibited strong and diffuse expression of all ISC markers, which indicate a stem cell‐like phenotype. However, normal colonic mucosa, hyperplastic polyps and sessile serrated adenomas harboured LGR 5 + cells that were confined to the crypt base and demonstrated an organized expression of ISC markers. Notably, in traditional serrated adenomas, expression of LGR 5 and ASCL 2 was localized to the ectopic crypts as in the normal crypts, but expression of EPHB 2 and OLFM 4 was distributed in a diffuse manner, which is suggestive of a progenitor‐like features. Conclusions The expression and distribution profile of ISC markers possibly provides insights into the organization of stem and progenitor‐like cells in each type of precancerous lesion of CRC .
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