CLEC1B Expression and PD-L1 Expression Predict Clinical Outcome in Hepatocellular Carcinoma with Tumor Hemorrhage

Kuan Hu; Zhi-Ming Wang; Juan-Ni Li; Sai Zhang; Zhong-Fu Xiao; Yi-Ming Tao

doi:10.1016/j.tranon.2018.02.010

CLEC1B Expression and PD-L1 Expression Predict Clinical Outcome in Hepatocellular Carcinoma with Tumor Hemorrhage

Transl Oncol. 2018 Apr;11(2):552-558. doi: 10.1016/j.tranon.2018.02.010. Epub 2018 Mar 8.

Authors

Kuan Hu¹, Zhi-Ming Wang¹, Juan-Ni Li², Sai Zhang³, Zhong-Fu Xiao⁴, Yi-Ming Tao⁵

Affiliations

¹ Department of Hepatobiliary Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
² Department of Pathology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
³ Institute of Medical Sciences, Xiangya Hospital, Central South University, Changsha, Hunan, China.
⁴ Department of Anesthesiology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
⁵ Department of Hepatobiliary Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China. Electronic address: yimingtao@csu.edu.cn.

Abstract

Spontaneous tumor hemorrhage (TH) is frequently observed in solid tumors including human hepatocellular carcinoma (HCC). TH implies fast-growing and worse tumor immunological microenvironment; however, the underlying mechanism remains largely unknown. CLEC1B is a signature gene highly associated with tumor progression. PD-L1 expression is a key biomarker predictive of immune checkpoint therapies, which showed astonishing effect on various types of tumor. We assume that, in HCC, TH may closely associate with the expression of these two molecules. In this study, 136 patients with HCC were enrolled. qRT-PCR showed that CLEC1B expression is significantly lower in HCC tumor tissue. Immunohistochemistry of HCC tissue microarrays demonstrated that PD-L1_high and CLEC1B_low expressions were significantly correlated with TH and clinicopathological features indicating worse HCC progression. According to univariate/multivariate analysis, a combination of PD-L1_high and CLEC1B_low expression was an independent prognostic factor indicating the poor outcome. The prognostic value of PD-L1_high and CLEC1B_low was validated by Cox proportional-hazard analyses. Collectively, tumor with TH is closely associated with CLEC1B_low & PD-L1_high expression, which may imply high response of PD-L1/PD-1 immune checkpoint therapies. CLEC1B may be a potential therapeutic target for PD-L1/PD-1 immunotherapy. PD-L1_high and CLEC1B_low can be a valuable prognosis factor implying worse clinical outcomes.