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人类异常隐窝病灶中单克隆性的鉴定。

The identification of monoclonality in human aberrant crypt foci.

作者信息

Siu I M, Robinson D R, Schwartz S, Kung H J, Pretlow T G, Petersen R B, Pretlow T P

机构信息

Institute of Pathology, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

Cancer Res. 1999 Jan 1;59(1):63-6.

PMID:9892186
Abstract

Malignant neoplasms, including colon cancers, are thought to arise from a single initiated progenitor cell. Aberrant crypt foci (ACF) are putative precursors of at least some colon cancers. The pattern of X chromosomal inactivation, which is identified by the differential methylation of a site near a polymorphic CAG repeat in the androgen receptor gene, was used to determine the clonality status of 11 ACF from eight female patients. Ten of 11 ACF were found to be monoclonal aberrations. The eleventh ACF appeared monoclonal, but nonrandom inactivation of the X chromosome was also seen in normal crypts from this patient. These results clearly demonstrate that: (a) a high percentage of ACF lesions are neoplastic rather than hyperplastic; and (b) ACF are the earliest identified neoplastic lesions in the colon.

摘要

恶性肿瘤,包括结肠癌,被认为起源于单个起始祖细胞。异常隐窝灶(ACF)被认为是至少部分结肠癌的推定前体。通过雄激素受体基因中多态性CAG重复序列附近位点的差异甲基化来鉴定的X染色体失活模式,被用于确定8名女性患者的11个ACF的克隆性状态。11个ACF中有10个被发现是单克隆畸变。第11个ACF看似是单克隆的,但在该患者的正常隐窝中也观察到了X染色体的非随机失活。这些结果清楚地表明:(a)高比例的ACF病变是肿瘤性的而非增生性的;(b)ACF是结肠中最早被鉴定出的肿瘤性病变。

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