Department of Experimental Analysis, Aerospace Medical Center, Republic of Korea Air Force, P.O. Box 335-21, 635 Danjae-ro, Namil-myeon, Cheongwon-gun, Chungcheongbuk-do 363-849, Republic of Korea.
Biomed Res Int. 2013;2013:527534. doi: 10.1155/2013/527534. Epub 2013 Jun 16.
Gallbladder carcinoma (GBCA) is one of the most aggressive malignancies. It is usually diagnosed at an advanced stage, and prognosis remains poor despite advances in imaging techniques and aggressive surgical treatment. Overexpression of multidrug resistance-associated proteins (MRPs) in tumor cells is a major cause of the intrinsic multidrug resistance phenotype. Despite the documented importance of MRP expression in many carcinomas, the prognostic significance of MRP2 expression in primary GBCA is not known. Immunostaining for MRP2 was performed on tissue samples obtained from 143 patients with GBCA. We examined the association between MRP expression and clinicopathological characteristics and outcome of patients with GBCA. GBCA demonstrated MRP2 immunoreactivity in the apicolateral membranes of epithelial cells. MRP2 expression was positive in 53.1% (76/143) of GBCA samples. Positive MRP2 expression was significantly associated with the presence of local recurrence (P = 0.038), lymphatic invasion (P = 0.038), vascular invasion (P = 0.023), and perineural invasion (P = 0.006). In addition, the median survival time of patients with MRP2-positive GBCA (15 months) was significantly shorter than that of patients with MRP2-negative GBCA (85 months, P = 0.011). We found that the expression of MRP2 in GBCA contributed to aggressive tumor behavior and poor prognosis, suggesting that MRP2 expression can be used as a potential prognostic biomarker of GBCA.
胆囊癌(GBCA)是最具侵袭性的恶性肿瘤之一。它通常在晚期被诊断出来,尽管影像学技术和积极的手术治疗有所进步,但预后仍然很差。肿瘤细胞中多药耐药相关蛋白(MRPs)的过度表达是内在多药耐药表型的主要原因。尽管 MRP 表达在许多癌中的重要性已有记录,但 MRP2 在原发性 GBCA 中的表达对预后的意义尚不清楚。对 143 例 GBCA 患者的组织样本进行了 MRP2 免疫组化染色。我们研究了 MRP 表达与 GBCA 患者的临床病理特征和结局之间的关系。GBCA 在上皮细胞的 apical 侧膜上显示出 MRP2 免疫反应性。在 143 例 GBCA 样本中,MRP2 表达阳性率为 53.1%(76/143)。MRP2 表达阳性与局部复发(P = 0.038)、淋巴血管侵犯(P = 0.038)、血管侵犯(P = 0.023)和神经周围侵犯(P = 0.006)显著相关。此外,MRP2 阳性 GBCA 患者的中位生存时间(15 个月)明显短于 MRP2 阴性 GBCA 患者(85 个月,P = 0.011)。我们发现,GBCA 中 MRP2 的表达导致了侵袭性肿瘤行为和不良预后,表明 MRP2 表达可以作为 GBCA 的潜在预后生物标志物。