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p16INK4a和p21Waf1基因的缺失及表达缺失与套细胞淋巴瘤的侵袭性变体相关。

Deletions and loss of expression of p16INK4a and p21Waf1 genes are associated with aggressive variants of mantle cell lymphomas.

作者信息

Pinyol M, Hernandez L, Cazorla M, Balbín M, Jares P, Fernandez P L, Montserrat E, Cardesa A, Lopez-Otín C, Campo E

机构信息

Department of Anatomic Pathology, Hospital Clinic Provincial, University of Barcelona, Spain.

出版信息

Blood. 1997 Jan 1;89(1):272-80.

PMID:8978301
Abstract

Mantle cell lymphoma (MCL) is molecularly characterized by bcl-1 rearrangement and cyclin D1 gene overexpression. Some aggressive variants of MCL have been described with blastic or large cell morphology, higher proliferative activity, and shorter survival. The cyclin-dependent kinase inhibitors (CDKIs) p21Waf1 and p16INK4a have been suggested as candidates for tumor-suppressor genes. To determine the role of p21Waf1 and p16INK4a gene alterations in MCLs, we examined the expression, deletions, and mutations of these genes in a series of 24 MCLs, 18 typical, and 6 aggressive variants. Loss of expression and/or deletions of p21Waf1 and p16INK4a genes were detected in 4 (67%) aggressive MCLs but in none of the typical variants. Two aggressive MCLs showed a loss of p16INK4a expression. These cases showed homozygous deletions of p16INK4a gene by Southern blot analysis. An additional aggressive MCL in which expression could not be examined showed a hemizygous 9p12 deletion. Loss of p21Waf1 expression at both protein and mRNA levels was detected in an additional aggressive MCL. No p21Waf1 gene deletions or mutations were found in this case. The p21Waf1 expression in MCLs was independent of p53 mutations. The two cases with p53 mutations showed p21Waf1 and p16INK4a expression whereas the 4 aggressive MCLs with p16INK4a and p21Waf1 gene alterations had a wild-type p53. p21Waf1 and p16INK4a were expressed at mRNA and protein levels in all typical MCLs examined. No gene deletions or point mutations were found in typical variants. Two typical MCLs showed an anomalous single-stranded conformation polymorphism corresponding to the known polymorphisms at codon 148 of p16INK4a gene and codon 31 of p21Waf1 gene. These findings indicate that p21Waf1 and p16INK4a alterations are rare in typical MCLs but the loss of p21Waf1 and p16INK4a expression, and deletions of p16INK4a gene are associated with aggressive variants of MCLs, and they occur in a subset of tumors with a wild-type p53 gene.

摘要

套细胞淋巴瘤(MCL)的分子特征为bcl-1重排和细胞周期蛋白D1基因过表达。已描述了一些具有母细胞样或大细胞形态、较高增殖活性及较短生存期的侵袭性MCL变异型。细胞周期蛋白依赖性激酶抑制剂(CDKIs)p21Waf1和p16INK4a被认为是肿瘤抑制基因的候选者。为确定p21Waf1和p16INK4a基因改变在MCL中的作用,我们检测了24例MCL(18例典型型和6例侵袭性变异型)中这些基因的表达、缺失及突变情况。在4例(67%)侵袭性MCL中检测到p21Waf1和p16INK4a基因表达缺失和/或缺失,但在所有典型变异型中均未检测到。2例侵袭性MCL显示p16INK4a表达缺失。Southern印迹分析显示这些病例p16INK4a基因纯合缺失。另一例无法检测表达的侵袭性MCL显示9p12半合子缺失。在另一例侵袭性MCL中检测到p21Waf1在蛋白和mRNA水平均表达缺失。该病例未发现p21Waf1基因缺失或突变。MCL中p21Waf1的表达与p53突变无关。2例p53突变的病例显示p21Waf1和p16INK4a表达,而4例具有p16INK4a和p21Waf1基因改变的侵袭性MCL具有野生型p53。在所有检测的典型MCL中,p21Waf1和p16INK4a在mRNA和蛋白水平均有表达。在典型变异型中未发现基因缺失或点突变。2例典型MCL显示与p16INK4a基因第148密码子和p21Waf1基因第31密码子已知多态性相对应的异常单链构象多态性。这些发现表明,p21Waf1和p16INK4a改变在典型MCL中罕见,但p21Waf1和p16INK4a表达缺失及p16INK4a基因缺失与MCL的侵袭性变异型相关,且它们发生在一部分具有野生型p53基因的肿瘤中。

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