Computer-aided assessment of the chemokine receptors CXCR3, CXCR4 and CXCR7 expression in gallbladder carcinoma

被引:3
|
作者
Yu, Xiao [1 ]
Lu, Wei [2 ,3 ]
Ng, Chan Way [4 ]
Xu, Shuoyu [5 ]
Wu, Yao [4 ]
Chen, Shili [3 ]
Gao, Yuren [6 ]
Zhang, Yijian [3 ]
Zhang, Qingqing [1 ]
Xu, Yuzhen [7 ]
Liu, Yingbin [2 ,3 ]
Li, Sheng [8 ]
机构
[1] Dalian Med Univ, Dept Pathol & Forens Med, Dalian, Peoples R China
[2] Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Dept Gen Surg, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Inst Biliary Tract Dis Res, Sch Med, Shanghai, Peoples R China
[4] Invitrocue Pte Ltd, Singapore, Singapore
[5] Sun Yat Sen Univ, Dept Radiol, Canc Ctr, Guangzhou, Peoples R China
[6] Dalian Med Univ, Dept Urol, Affiliated Hosp 2, Dalian, Peoples R China
[7] Southeast Univ, Xu Zhou Ctr Hosp, Dept Gastrointestinal Surg, Med Coll, Xuzhou, Jiangsu, Peoples R China
[8] Dalian Med Univ, Natl Local Engn Res Ctr Drug Res & Dev R&D Neurod, Dept Biochem, Lvshun South Rd 9, Dalian 116044, Peoples R China
关键词
computer-aided; CXCR3; CXCR4; CXCR7; gallbladder cancer; quantitative assessment; MANAGEMENT; SURVIVAL; CANCER;
D O I
10.1111/jcmm.15219
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gallbladder carcinoma (GBC) is a vicious and invasive disease. The major challenge in the clinical treatment of GBC is the lack of a suitable prognosis method. Chemokine receptors such as CXCR3, CXCR4 and CXCR7 play vital roles in the process of tumour progression and metastasis. Their expression levels and distribution are proven to be indicative of the progression of GBC, but are hard to be decoded by conventional pathological methods, and therefore, not commonly used in the prognosis of GBC. In this study, we developed a computer-aided image analysis method, which we used to quantitatively measure the expression levels of CXCR3, CXCR4 and CXCR7 in the nuclei and cytoplasm of glandular and interstitial cells from a cohort of 55 GBC patients. We found that CXCR3, CXCR4 and CXCR7 expressions are associated with the clinicopathological variables of GBC. Cytoplasmic CXCR3, nuclear CXCR7 and cytoplasmic CXCR7 were significant predictive factors of histology invasion, whereas cytoplasmic CXCR4 and nuclear CXCR4 were significantly correlated with T and N stage and were associated with the overall survival and disease-free survival. These results suggest that the quantification and localisation of CXCR3, CXCR4 and CXCR7 expressions in different cell types should be considered using computer-aided assessment to improve the accuracy of prognosis in GBC.
引用
收藏
页码:7670 / 7674
页数:5
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