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家族性脆性8号染色体q22区在一例大肠肿瘤细胞中作为癌症断点被涉及。

Familial fragile 8q22 involved as a cancer breakpoint in cells of a large bowel tumor.

作者信息

Shabtai F, Sternberg A, Klar D, Halbrecht I, Reiss R

机构信息

Gattegno Research Institute, Hasharon Hospital, Petah Tikva, Israel.

出版信息

Cancer Genet Cytogenet. 1988 Mar;31(1):113-8. doi: 10.1016/0165-4608(88)90018-0.

Abstract

A familial fragile 8q22 and an interferon-induced fragile 16q22 were found in two sisters. Eight years previously, both sisters developed an endometrial adenocarcinoma and now one of them presented with an adenocarcinoma of the colon. An 8q22 deletion was found in all the cells of the colonic tumor and seemed to be the primary initiating change. Other nonrandom and possibly promoting aberrations were also present, among others, a 16q22 deletion. The possibility exists that a familial fragile 8q22 may predispose to cancer and a fragile 16q22 may have promoting capacities.

摘要

在两姐妹中发现了家族性脆性8q22和干扰素诱导的脆性16q22。八年前,两姐妹均患子宫内膜腺癌,现在其中一人又患结肠癌。在结肠肿瘤的所有细胞中均发现8q22缺失,这似乎是主要的起始变化。还存在其他非随机性且可能具有促进作用的畸变,其中包括16q22缺失。家族性脆性8q22可能易患癌症,而脆性16q22可能具有促进癌症发生发展的能力。

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