Lee Yu-Chieh, Su Chia-Yu, Lin Yuan-Feng, Lin Chun-Mao, Fang Chih-Yeu, Lin Yen-Kuang, Hsiao Michael, Chen Chi-Long
Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Division of Gastroenterology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, Taipei, Taiwan.
Oncotarget. 2017 Feb 14;8(7):12120-12132. doi: 10.18632/oncotarget.14552.
Colorectal cancer (CRC) is one of the leading cancers worldwide. Surgery is the main therapeutic modality for stage II CRC. However, the implementation of adjuvant chemotherapy remains controversial and is not universally applied so far. In this study, we found that the protein expression of lysosomal acid phosphatase 2 (ACP2) was increased in CRC and that stage II CRC patients with high ACP2 expression showed a poorer outcome than those with low ACP2 expression (p = 0.004). To investigate this discrepancy, we analyzed the relation between ACP2 expression and several clinical cofactors.Among patients who received chemotherapy, those with an high expression of ACP2 showed better survival in both stage II and III CRC than those with low ACP2 expression. In stage II CRC patients, univariate analysis showed ACP2 expression and T stage to be cofactors significantly associated with overall survival (ACP2: p = 0.006; T stage: p = 0.034). Multivariate Cox proportion hazard model analysis also revealed ACP2 to be an independent prognostic factor for overall survival (ACP2: p = 0.006; T stage: p = 0.041). Furthermore, ACP2-knockdown CRC cells showed an increase in chemoresistance to 5-FU treatment and increased proliferation marker in the ACP2 knockdown clone.Taken together, our results suggested that ACP2 is an unfavorable prognostic factor for stage II CRC and may serve as a potential chemotherapy-sensitive marker to help identify a subset of stage II and III CRC patients for whom chemotherapy would improve survival.Highlights1. To the best of our knowledge, the study is the first report to show ACP2 overexpression in human colorectal cancer (CRC) and its association with poor outcome in stage II CRC.2. Patients with stage II and III CRCs with high expression of ACP2 were more sensitive to chemotherapy than those with a low expression.3. ACP2 expression may serve as a marker for CRC patients receiving chemotherapy and help identify the subset of CRC patients who would benefit from chemotherapy.
结直肠癌(CRC)是全球主要癌症之一。手术是II期CRC的主要治疗方式。然而,辅助化疗的应用仍存在争议,目前尚未普遍应用。在本研究中,我们发现溶酶体酸性磷酸酶2(ACP2)在CRC中的蛋白表达增加,且II期CRC患者中ACP2高表达者的预后比低表达者差(p = 0.004)。为研究这种差异,我们分析了ACP2表达与几种临床辅助因素之间的关系。在接受化疗的患者中,ACP2高表达的II期和III期CRC患者的生存率均高于低表达者。在II期CRC患者中,单因素分析显示ACP2表达和T分期是与总生存显著相关的辅助因素(ACP2:p = 0.006;T分期:p = 0.034)。多因素Cox比例风险模型分析也显示ACP2是总生存的独立预后因素(ACP2:p = 0.006;T分期:p = 0.041)。此外,敲低ACP2的CRC细胞对5-FU治疗的化疗耐药性增加,且在敲低ACP2的克隆中增殖标志物增加。综上所述,我们的结果表明,ACP2是II期CRC的不良预后因素,可能作为潜在的化疗敏感性标志物,以帮助识别II期和III期CRC患者中化疗可改善生存的亚组。重点内容:1. 据我们所知,本研究是首次报道人结直肠癌(CRC)中ACP2过表达及其与II期CRC不良预后的关联。2. ACP2高表达的II期和III期CRC患者比低表达患者对化疗更敏感。3. ACP2表达可作为接受化疗的CRC患者的标志物,并有助于识别将从化疗中获益的CRC患者亚组。