The Role of Jianpi Jiedu Recipe in Modulating the CRC Microenvironment.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Mengyao Li, Dongming Hua, Yuanyuan Feng, Zhiyan Wang, Xueqing Hu, Yan Wang
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引用次数: 0

Abstract

Background: The anti-tumor effects of Traditional Chinese Medicine has been recognized in regulating the tumor microenvironment. Jianpi Jiedu Recipe (JPJDR) is clinically effective in enhancing the chemotherapy efficacy in Colorectal Cancer (CRC) treatment and significantly improved the quality of life of CRC patients. However, its therapeutic mechanism remains to be investigated.

Material and methods: The active compounds of each herb in JPJDR were obtained from the HIT2.0 and HERB databases supported by evidence in literature. Single-cell RNA sequencing data of CRC were obtained from published studies (PMID: 32451460, 32103181, and 32561858). Pathway enrichment was analyzed using the reactome database, and gene correlation analysis was performed using the corrplot R software package. Gene expression regulated by JPJDR was verified by RT-qPCR.

Results: Ye Pu Tao Teng, Ba Yue Zha, Huang Qi, Bai Zhu, Yi Yi Ren and Dang Shen contained 4,7, 18, 26,3 and 30 compounds, respectively, and they target to 38, 7, 262, 309, 50, 54 genes, respectively. JPJDR is involved in a range of immune-related biological processes, including cytokine signaling, cell proliferation, apoptosis and cellular senescence. JPJDR regulates various cell types in the CRC microenvironment, including malignant CRC cells, immune cells (including CD4+ T cell, CD8+ T cell, B cell, plasma cell, mast cell, and myeloid cell), and stromal cells (including fibroblast, pericyte, enteric glial cell, and endothelial cell). We confirmed that JPJDR significantly downregulated the expression of HMGB1 and MT2A in CRC.

Conclusions: JPJDR regulates a range of cell types in the CRC microenvironment, including malignant CRC, immune cells and stromal cells. Downregulation of HMGB1 and MT2A might be the important mediators for JPJDR to modulate the CRC microenvironment.

健脾解毒方对CRC微环境的调节作用。
背景:中药在调节肿瘤微环境方面的抗肿瘤作用已被公认。健脾解毒方(JPJDR)在临床上可有效提高结直肠癌(CRC)治疗的化疗疗效,显著改善结直肠癌患者的生活质量。然而,其治疗机制仍有待研究。材料与方法:JPJDR中各中药有效成分均从HIT2.0和herb数据库中检索,并有文献支持。CRC的单细胞RNA测序数据来自已发表的研究(PMID: 32451460, 32103181和32561858)。使用reactome数据库分析Pathway富集,使用corrplot R软件包进行基因相关性分析。通过RT-qPCR验证JPJDR调控的基因表达。结果:叶蒲桃藤、八月扎、黄芪、白竹、一益仁和当神分别含有4、7、18、26、3和30个化合物,分别靶向38、7、262、309、50和54个基因。JPJDR参与一系列免疫相关的生物学过程,包括细胞因子信号传导、细胞增殖、细胞凋亡和细胞衰老。JPJDR调节结直肠癌微环境中的多种细胞类型,包括恶性结直肠癌细胞、免疫细胞(包括CD4+ T细胞、CD8+ T细胞、B细胞、浆细胞、肥大细胞和髓样细胞)和基质细胞(包括成纤维细胞、周细胞、肠胶质细胞和内皮细胞)。我们证实JPJDR显著下调了CRC中HMGB1和MT2A的表达。结论:JPJDR调控结直肠癌微环境中的多种细胞类型,包括恶性结直肠癌、免疫细胞和基质细胞。HMGB1和MT2A的下调可能是JPJDR调控CRC微环境的重要介质。
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来源期刊
CiteScore
3.10
自引率
5.60%
发文量
327
审稿时长
7.5 months
期刊介绍: Combinatorial Chemistry & High Throughput Screening (CCHTS) publishes full length original research articles and reviews/mini-reviews dealing with various topics related to chemical biology (High Throughput Screening, Combinatorial Chemistry, Chemoinformatics, Laboratory Automation and Compound management) in advancing drug discovery research. Original research articles and reviews in the following areas are of special interest to the readers of this journal: Target identification and validation Assay design, development, miniaturization and comparison High throughput/high content/in silico screening and associated technologies Label-free detection technologies and applications Stem cell technologies Biomarkers ADMET/PK/PD methodologies and screening Probe discovery and development, hit to lead optimization Combinatorial chemistry (e.g. small molecules, peptide, nucleic acid or phage display libraries) Chemical library design and chemical diversity Chemo/bio-informatics, data mining Compound management Pharmacognosy Natural Products Research (Chemistry, Biology and Pharmacology of Natural Products) Natural Product Analytical Studies Bipharmaceutical studies of Natural products Drug repurposing Data management and statistical analysis Laboratory automation, robotics, microfluidics, signal detection technologies Current & Future Institutional Research Profile Technology transfer, legal and licensing issues Patents.
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