Department of Anatomical Pathology, Concord Hospital, The University of Sydney, Sydney, New South Wales, Australia.
Histopathology. 2011 Dec;59(6):1057-70. doi: 10.1111/j.1365-2559.2011.04044.x.
This study investigated the association between glutathione S-transferase Pi (GST Pi) expression, histopathology and overall survival in 468 patients after resection of stage C colonic adenocarcinoma.
Data were drawn from a prospective hospital registry of consecutive bowel cancer resections with a minimum follow-up of 5 years. Nuclear and cytoplasmic GST Pi expression, assessed by both intensity of staining and percentage of stained cells at both the central part of the tumour and the invasive tumour front, were evaluated retrospectively by tissue microarray immunohistochemistry on archival specimens. The most effective measure of GST Pi expression was the percentage of immunostained nuclei in central tumour tissue, where >40% stained was associated significantly with high grade, invasion beyond the muscularis propria, involvement of a free serosal surface or apical node, and invasion into an adjacent organ or structure. After adjustment of other predictors, GST Pi expression remained independently prognostic for reduced overall survival (hazard ratio 1.4, P = 0.002).
In patients with clinicopathological stage C colonic cancer, GST Pi expression is associated with features of tumour aggressiveness and with reduced overall survival. Further appropriately designed studies should aim to discover whether GST Pi can predict response to adjuvant chemotherapy.
本研究调查了谷胱甘肽 S-转移酶 Pi(GST Pi)表达、组织病理学和 468 例 C 期结肠腺癌切除术后总生存期之间的关系。
数据来自连续进行的肠道癌症切除术的前瞻性医院登记处,随访时间至少为 5 年。通过组织微阵列免疫组织化学在存档标本上回顾性评估核和细胞质 GST Pi 表达,通过染色强度和肿瘤中央部分及浸润性肿瘤前缘染色细胞的百分比来评估。GST Pi 表达的最有效衡量标准是中央肿瘤组织中免疫染色核的百分比,其中>40%染色与高级别、超出肌肉层的浸润、游离浆膜表面或顶端节点的受累以及侵入相邻器官或结构显著相关。在调整其他预测因素后,GST Pi 表达仍然是总生存期降低的独立预后因素(风险比 1.4,P = 0.002)。
在临床病理分期为 C 期的结肠癌患者中,GST Pi 表达与肿瘤侵袭性特征和总生存期降低相关。进一步进行适当设计的研究应旨在发现 GST Pi 是否可以预测辅助化疗的反应。