de Jong Koert P, Gouw Annette S H, Peeters Paul M J G, Bulthuis Marian, Menkema Lorian, Porte Robert J, Slooff Maarten J H, van Goor Harry, van den Berg Anke
Division of Hepato-Pancreato-Biliary Surgery and Liver Transplantation, Department of Surgery, University Medical Center Groningen, Groningen, the Netherlands.
Clin Cancer Res. 2005 Jun 1;11(11):4067-73. doi: 10.1158/1078-0432.CCR-04-2389.
To correlate TP53 mutations with angiogenic status of the tumor and prognosis after liver surgery in patients with colorectal liver metastases and to correlate immunohistochemical staining of p53 protein with TP53 gene mutations.
Tumors of 44 patients with surgically treated colorectal liver metastases were analyzed for (a) TP53 mutations using denaturing gradient gel electrophoresis followed by sequencing, (b) microvessel density using the hot spot overlap technique, (c) apoptotic rate in tumor cells and endothelial cells of tumor microvessels using double immunostaining for anti-cleaved caspase 3 and anti-CD34, and (d) expression of p53 protein using immunohistochemistry.
TP53 mutations were detected in 36% of the metastases and occurred more frequently in liver metastases from left-sided colon tumors than from right-sided colon tumors (P = 0.04). In metastases with TP53 mutations, microvessel density was higher compared with tumors with wild-type p53. Endothelial cell apoptosis was not different in tumor microvessels from TP53-mutated versus nonmutated tumors. The 5-year actual survival was not influenced by TP53 mutational status, microvessel density, or endothelial cell apoptotic rate of the tumors. Based on immunohistochemical p53 overexpression, the positive and negative predictive values of TP53 mutations were 61% and 82%.
In patients with surgically treated colorectal liver metastases, TP53 mutations and angiogenic status did not influence prognosis. Immunohistochemistry is not a reliable technique for detecting TP53 mutations.
探讨结直肠癌肝转移患者肝切除术后TP53突变与肿瘤血管生成状态及预后的相关性,并分析p53蛋白免疫组化染色与TP53基因突变的相关性。
对44例接受手术治疗的结直肠癌肝转移患者的肿瘤进行分析,包括:(a)采用变性梯度凝胶电泳及测序检测TP53突变;(b)采用热点重叠技术检测微血管密度;(c)采用抗裂解型半胱天冬酶3和抗CD34双重免疫染色检测肿瘤微血管中肿瘤细胞和内皮细胞的凋亡率;(d)采用免疫组化检测p53蛋白表达。
36%的转移灶检测到TP53突变,左侧结肠癌肝转移灶的TP53突变发生率高于右侧结肠癌肝转移灶(P = 0.04)。与野生型p53肿瘤相比,TP53突变的转移灶微血管密度更高。TP53突变与未突变肿瘤的微血管内皮细胞凋亡无差异。肿瘤的TP53突变状态、微血管密度或内皮细胞凋亡率均不影响5年实际生存率。基于免疫组化p53过表达,TP53突变的阳性和阴性预测值分别为61%和82%。
在接受手术治疗的结直肠癌肝转移患者中,TP53突变和血管生成状态不影响预后。免疫组化不是检测TP53突变的可靠技术。