Henderson-Jackson Evita B, Helm James, Ghayouri Masoumeh, Hakam Ardeshir, Nasir Aejaz, Leon Marino, Bui Marilyn, Yeatman Timothy, Coppola Domenico
Departments of Oncologic Sciences; Moffitt Cancer Center and Research Institute, at the University of South Florida, School of Medicine, Tampa, Florida 33612-3275, USA
Int J Clin Exp Pathol. 2010 Oct 12;3(8):768-74.
Mcl-1 inhibits apoptosis in well-differentiated cells by sequestering BAD, BID, and BAX and other apoptotic molecules. pAKT blocks apoptotsis by facilitating the interaction of BAD with BCL-XL. Expression of pAKT and Mcl-1 have been described in colon cancer, however, the relationship between pAKT and Mcl-1 has not. Mcl-1 and pAKT immunohistochemistry was performed using colorectal cancer tissue microarray (TMA). The Holm step-down method was used to adjust for multiple testing. Mcl-1 and pAKT scores, stage, and grade were compared using Spearman's correlation coefficient. Metastasis and no metastasis groups were compared using the Wilcoxon rank sum test. Mcl-1 and pAKT scores were compared for normal colorectal mucosa (NR), adenoma (AD), and colorectal cancer (CRC) cohorts. The mean (SD) pAKT expression in NR (14) was 2.0 (1.4), in AD (8) was 3.0 (1.7), and in CRC (101) was 5.6 (2.4). These differences were statistically significant. For Mcl-1 the mean (SD) expression was 4.1 (1.7) in NR, 3.2 (1.2) in AD, and 3.3 (2.6) in CRC. Mcl-1 and pAKT scores were directly correlated during various stages of colon car-cinogenesis (p = 0.04). Mcl-1 showed direct correlation with tumor grade (p = 0.001) and tumor stage (p = 0.02) and with presence of metastasis (p = 0.008). We report the correlation of Mcl-1 protein expression with higher grade and stage in colorectal cancer. Mcl-1 correlated also with pAKT expression. We also report the up regulation of pAKT during the transition from NR to CRC.
髓细胞白血病-1(Mcl-1)通过隔离BAD、BID和BAX以及其他凋亡分子来抑制分化良好细胞中的凋亡。磷酸化蛋白激酶B(pAKT)通过促进BAD与BCL-XL的相互作用来阻断凋亡。pAKT和Mcl-1在结肠癌中的表达已有报道,然而,pAKT与Mcl-1之间的关系尚未见报道。使用结直肠癌组织微阵列(TMA)进行Mcl-1和pAKT免疫组织化学检测。采用霍尔姆逐步下调法进行多重检验校正。使用斯皮尔曼相关系数比较Mcl-1和pAKT评分、分期和分级。使用威尔科克森秩和检验比较转移组和非转移组。比较正常结直肠黏膜(NR)、腺瘤(AD)和结直肠癌(CRC)队列的Mcl-1和pAKT评分。NR组(14例)中pAKT的平均(标准差)表达为2.0(1.4),AD组(8例)为3.0(1.7),CRC组(101例)为5.6(2.4)。这些差异具有统计学意义。对于Mcl-1,NR组的平均(标准差)表达为4.1(1.7),AD组为3.2(1.2),CRC组为3.3(2.6)。在结肠癌发生的各个阶段,Mcl-1和pAKT评分直接相关(p = 0.04)。Mcl-1与肿瘤分级(p = 0.001)、肿瘤分期(p = 0.02)以及转移的存在(p = 0.008)呈直接相关。我们报道了Mcl-1蛋白表达与结直肠癌更高分级和分期的相关性。Mcl-1也与pAKT表达相关。我们还报道了从NR到CRC转变过程中pAKT的上调。