Authors' Affiliations: Departments of Breast Surgery, and Pathology, Fudan University Shanghai Cancer Center/Cancer Institute; Department of Oncology, Shanghai Medical College; and Institutes of Biomedical Science, Fudan University, Shanghai, PR China.
Clin Cancer Res. 2013 Dec 15;19(24):6853-62. doi: 10.1158/1078-0432.CCR-13-1617. Epub 2013 Oct 18.
This study sought to investigate the prognostic value of the autophagy marker microtubule-associated protein chain 3B (LC3B) in patients with residual tumors after neoadjuvant chemotherapy (NCT) for locally advanced breast cancer (LABC).
The expression of LC3B in residual breast cancer cells was assessed by immunohistochemistry in surgical specimens from 229 patients diagnosed with histologically proven invasive breast cancer. All patients underwent NCT followed by mastectomy and were considered nonpathologic complete responders (non-pCR) after a pathologic evaluation. The prognostic value of various clinicopathologic factors was evaluated.
The LC3B density was similar between the peripheral and central area of the tumors (P = 0.328) but was significantly lower in the extratumoral area (P < 0.001 and P < 0.001, respectively). Furthermore, LC3B density, which correlated with Beclin-1 expression, Ki-67 index, and breast cancer subtype, served as an independent prognostic factor for both relapse-free survival (RFS; P = 0.012) and overall survival (OS; P = 0.008); the prognostic value of LC3B was most significant in triple-negative patients. Using a combination of LC3B expression and the status of residual involved lymph nodes, the patients were classified into four groups with different risks of relapse and death (P < 0.001 for RFS and P = 0.003 for OS).
LC3B can be used as a prognostic marker in patients with non-pCR after NCT for breast cancer, which highlights the importance of autophagy in the biologic behavior of chemoresistant cancer cells. Furthermore, evaluating and targeting autophagy in the neoadjuvant setting may help prevent disease relapse in patients with non-pCR.
本研究旨在探讨自噬标志物微管相关蛋白轻链 3B(LC3B)在接受新辅助化疗(NCT)后局部晚期乳腺癌(LABC)患者残留肿瘤中的预后价值。
通过免疫组织化学评估 229 例经组织学证实为浸润性乳腺癌患者手术标本中残留乳腺癌细胞中 LC3B 的表达。所有患者均接受 NCT 治疗,随后行乳房切除术,经病理评估后被认为是非病理完全缓解者(non-pCR)。评估了各种临床病理因素的预后价值。
肿瘤外周区和中央区的 LC3B 密度相似(P=0.328),但肿瘤外区的 LC3B 密度显著降低(分别为 P<0.001 和 P<0.001)。此外,LC3B 密度与 Beclin-1 表达、Ki-67 指数和乳腺癌亚型相关,是无复发生存(RFS;P=0.012)和总生存(OS;P=0.008)的独立预后因素;LC3B 的预后价值在三阴性患者中最为显著。通过 LC3B 表达和残留受累淋巴结状态的组合,将患者分为四个具有不同复发和死亡风险的组(RFS 为 P<0.001,OS 为 P=0.003)。
LC3B 可作为 NCT 后非 pCR 乳腺癌患者的预后标志物,这突出了自噬在化疗耐药癌细胞生物学行为中的重要性。此外,在新辅助治疗中评估和靶向自噬可能有助于预防非 pCR 患者的疾病复发。