Association of beclin 1 expression with response to neoadjuvant chemoradiation therapy in patients with locally advanced rectal carcinoma

被引:26
作者
Zaanan, Aziz [1 ,2 ]
Park, Jae Myung [1 ,2 ]
Tougeron, David [1 ,2 ]
Huang, Shengbing [1 ,2 ]
Wu, Tsung-Teh [2 ,3 ]
Foster, Nathan R. [2 ,4 ]
Sinicrope, Frank A. [1 ,2 ,5 ]
机构
[1] Mayo Clin, Dept Med, Rochester, MN 55905 USA
[2] Mayo Canc Ctr, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Pathol & Lab Med, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Biomed Stat & Informat, Rochester, MN 55905 USA
[5] Mayo Clin, Dept Oncol, Rochester, MN 55905 USA
关键词
beclin; 1; rectal cancer; chemoradiation; autophagy; biomarker; PATHOLOGICAL COMPLETE RESPONSE; POSTOPERATIVE CHEMORADIOTHERAPY; PREOPERATIVE CHEMORADIATION; PROGNOSTIC IMPACT; CANCER; AUTOPHAGY; 5-FLUOROURACIL; RADIOTHERAPY; INHIBITION; RESISTANCE;
D O I
10.1002/ijc.29496
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Beclin 1 is an essential regulator of autophagy that is induced in response to cellular stress and serves to maintain cell survival in established tumors. We recently demonstrated that Beclin 1 suppression can sensitize colorectal cancer cells to radiation-induced DNA damage and apoptosis. Therefore, we hypothesized that the level of Beclin 1 expression may be associated with radiation sensitivity in vivo. We determined the association of Beclin 1 expression in pretreatment rectal cancer tissues with response to neoadjuvant chemoradiation in surgical resection specimens. Stages II and III (n=96) rectal adenocarcinoma patients were treated with neoadjuvant chemoradiation followed by surgical resection with curative intent. Beclin 1 was analyzed by immunohistochemistry and the expression level was dichotomized at the median value with categorization into low and high groups. We identified 56 (58.3%) and 40 (41.7%) patients whose tumors had high- versus low-level Beclin 1 expression, respectively. Rectal cancers with high versus low Beclin 1 expression were significantly less likely to be downstaged after chemoradiation treatment (45% [25/55] vs. 58% [22/38]; p=0.02). In a multivariable analysis adjusted for age, sex, histological grade and baseline tumor node metastasis (TNM) stage, the impact of Beclin 1 expression on tumor downstaging remained statistically significant (p=0.03). The association of the level of Beclin 1 expression with the rate of tumor downstaging after chemoradiation is consistent with in vitro data, and suggests that Beclin 1 may be a predictive biomarker for the efficacy of chemoradiation in patients with rectal cancer. What's new? Patients with nonmetastatic rectal cancer routinely receive chemotherapy and radiation before surgery. However, a predictive marker for the efficacy of chemoradiation is lacking. Here, the authors show that the essential autophagy protein Beclin 1 -known to protect against radiation-induced DNA damage- could be such a predictive marker. In locally advanced rectal cancer patients, high-level Beclin 1 expression in pretreatment tumor tissues was associated with a significantly reduced rate of tumor downstaging after chemoradiation and vice versa, supporting a new role of Beclin 1 as a clinical biomarker.
引用
收藏
页码:1498 / 1502
页数:5
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