CXCL9型
医学
内科学
肿瘤科
C-C趋化因子受体7型
免疫组织化学
肿瘤微环境
趋化因子受体
CCL19型
癌症
癌症研究
趋化因子
宫颈癌
CXCL10型
CXCR3型
受体
作者
Hascitha Jayakumar,Abirami Seetharaman,Shirley Sunder Singh,Hemavathi Dhandapani,Subramani Jayavelu,Selvaluxmy Ganeshrajah,Thangarajan Rajkumar,Priya Ramanathan
标识
DOI:10.1016/j.jri.2021.103454
摘要
The over expression of Indoleamine 2, 3-Dioxygenase (IDO1), an immune checkpoint inhibitor, is well known in cervical cancer. However, its association with chemokine signals promoting cellular infiltration in the cervical tumor microenvironment, is unknown. In the current study, we evaluated the expression and enzymatic activity of IDO1. We also profiled the expression of chemokine ligand-receptors- CCR4-CCL22, CXCR3-CXCL10, CXCR4-CXCL12, and CCR7-CCL19 using immunohistochemistry (IHC), and studied their association with IDO1, statistically. After getting an informed consent, punch biopsy samples were obtained from 105 patients diagnosed with cervical cancer. HPV typing by Sanger sequencing, realtime PCR for quantifying IDO1 mRNA expression, HPLC for determining the K/T ratio and IHC for all the above chemokine receptor-ligand pairs along with IDO1 were performed. We found a significant increase in the expression of IDO1 and K/T levels in early and locally advanced stages when compared to Stage IV disease. Among the chemokine ligand -receptor pairs profiled, we found that high CCL19 marker expression was a good prognostic indicator of patients' disease-free (p = 0.013) and overall survival (p = 0.043). Although we could not identify IDO1 as an independent prognostic factor, we found that high levels of IDO1 expression may further reduce survival outcomes in patients with low CCL19 expression. This could be vital for designing immuno therapeutic interventions targeting IDO1.
科研通智能强力驱动
Strongly Powered by AbleSci AI