扶正祛邪法干预肿瘤微环境作用机制研究进展
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  • 英文篇名:Research Progress on Mechanism of Strengthening Body Resistance to Eliminate Pathogenic Factors Method in the Intervention of Tumor Microenvironment
  • 作者:马仰仰 ; 李仁廷 ; 张洁 ; 马一鸣 ; 司海龙
  • 英文作者:MA Yangyang;LI Renting;ZHANG Jie;MA Yiming;SI Hailong;Shaanxi University of Chinese Medicine;Affiliated Hospital of Shaanxi University of Traditional Chinese Medicine;
  • 关键词:扶正祛邪法 ; 肿瘤微环境 ; 肿瘤相关巨噬细胞 ; 肿瘤相关成纤维细胞
  • 英文关键词:strengthening body resistance to eliminate pathogenic factors method;;tumor microenvironment;;tumor-associated macrophages;;carcinoma-associated fibroblasts
  • 中文刊名:LZXB
  • 英文刊名:Journal of Liaoning University of Traditional Chinese Medicine
  • 机构:陕西中医药大学;陕西中医药大学附属医院;
  • 出版日期:2019-03-29
  • 出版单位:辽宁中医药大学学报
  • 年:2019
  • 期:v.21;No.180
  • 基金:国家自然科学基金青年项目(81704066)
  • 语种:中文;
  • 页:LZXB201904029
  • 页数:5
  • CN:04
  • ISSN:21-1543/R
  • 分类号:101-105
摘要
近年来中医药调节肿瘤微环境的研究已成为中医药治疗恶性肿瘤的热点之一。运用扶正祛邪法对恶性肿瘤微环境的干预发挥了重要的作用。该文综合分析扶正祛邪法对恶性肿瘤微环境中肿瘤相关巨噬细胞和肿瘤相关成纤维细胞作用机制的研究,可为今后中医药干预恶性肿瘤治疗提供新的防治思路。
        In recent years,the research of Chinese medicine regulating tumor microenvironment has become one of the hot topics of traditional Chinese medicine in the treatment of malignant tumors. The application of strengthening body resistance to eliminate pathogenic factors has played an important role in the intervention of malignant tumor microenvironment. The mechanism of strengthening body resistance to eliminate pathogenic factors on tumor associated macrophages and tumor-associated fibroblasts in malignant tumor microenvironment is comprehensively analyzed in this paper,it can provide a new way of prevention and treatment for the treatment of malignant tumors in the future.
引文
[1]陈万青,郑荣寿,张思维,等. 2012年中国恶性肿瘤发病和死亡分析[J].中国肿瘤,2016,25(1):1-8.
    [2]Fidler I J. The pathogenesis of cancer metastasis:the'seed and soil'hypothesis revisited[J]. Nature Reviews Cancer,2003,3(6):453.
    [3]Sung S Y,Hsieh C L,Wu D,et al. Tumor microenvironment promotes cancer progression,metastasis,and therapeutic resistance[J]. Current Problems in Cancer,2007,31(2):36-100.
    [4]Chanmee T,Ontong P,Konno K,et al. Tumor-associated macrophages as major players in the tumor microenvironment[J].Cancers,2014,6(3):1670-1690.
    [5]Sewell-Loftin M K,Bayer S V H,Crist E,et al. Cancerassociated fibroblasts support vascular growth through mechanical force[J]. Scientific Reports,2017,7(1):12574.
    [6]Pollard J W. Tumour-educated macrophages promote tumour progression and metastasis[J]. Nature Reviews Cancer,2004,4(1):71-78.
    [7]Ohno S,Ohno Y,Suzuki N,et al. Correlation of histological localizationoftumor-associatedmacrophageswith clinicopathological features in endometrial cancer[J]. Anticancer Research,2004,24(5C):3335-3342.
    [8]Martinez-Outschoorn U E,Lin Z,Ko Y H,et al. Understanding the metabolic basis of drug resistance[J]. Cell Cycle,2011,10(15):8.
    [9]Sica A,Schioppa T,Mantovani A,et al. Tumour-associated macrophages are a distinct M2 polarised population promoting tumour progression:Potential targets of anti-cancer therapy[J].European Journal of Cancer,2006,42(6):1-727.
    [10]Yuri P,Hendri A Z,Danarto R,et al. Association between tumor-associated macrophages and microvessel density on prostate cancer progression[J]. Prostate International,2015,3(3):93-98.
    [11]Park J Y,Sung J Y,Lee J,et al. Polarized CD163+tumorassociatedmacrophagesareassociatedwithincreased angiogenesis and CXCL12 expression in gastric cancer[J]. Clin Res Hepatol Gastroenterol,2016,40(3):357-365.
    [12]MantovaniA,SozzaniS,LocatiM,etal.Macrophage polarization:tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes[J]. Trends in Immunology,2002,23(11):549-555.
    [13]Cruzleal Y,Lucatelli Laurindo M F,Osugui L,et al. Liposomes of phosphatidylcholine and cholesterol induce an M2-like macrophage phenotype reprogrammable to M1 pattern with the involvement of B-1 cells[J]. Immunobiology,2014,219(6):403-415.
    [14]LIU CY,XU JY,SHI XY,et al. M2-polarized tumor-associated macrophages promoted epithelial-mesenchymal transition in pancreatic cancer cells,partially through TLR4/IL-10 signaling pathway[J]. Laboratory Investigation,2013,93(7):844-854.
    [15]Yaddanapudi K,Putty K,Rendon B E,et al. Control of tumorassociated macrophage alternative activation by MIF[J]. Journal of Immunology,2013,190(6):2984.
    [16]Martinez F O,Gordon S,Locati M,et al. Transcriptional profiling of the human monocyte-to-macrophage differentiation and polarization:new molecules and patterns of gene expression[J]. Journal of Immunology,2006,177(10):7303-7311.
    [17]Schmid M C,Varner J A. Myeloid cells in tumor inflammation[J].Vascular Cell,2012,4(1):1-7.
    [18]Mantovani A,Sica A,Sozzani S,et al. The chemokine system in diverse forms of macrophage activation and polarization[J].Trends in Immunology,2004,25(12):677-686.
    [19]Gordon S. Alternative activation of macrophages[J]. Nature Reviews Immunology,2003,3(1):23-35.
    [20]H a o,N i n g B o,Lü,e ta l.M a c r o p h a g e si nt u m o r microenvironments and the progression of tumors[J]. Clinical&Developmental Immunology,2012,11(2014):948098.
    [21]Pollard J W. Tumour-educated macrophages promote tumour progression and metastasis[J]. Nature Reviews Cancer,2004,4(1):71-78.
    [22]Sica A. Macrophages,innate immunity and cancer:balance,tolerance,and diversity[J]. Current Opinion in Immunology,2010,22(2):231-237.
    [23]Van Ginderachter J A,Movahedi K,Hassanzadeh G G,et al.Classical and alternative activation of mononuclear phagocytes:picking the best of both worlds for tumor promotion[J].Immunobiology,2006,211(6-8):487.
    [24]Pikarsky E,Porat R M,Stein I,et al. NF-kappaB functions as a tumour promoter in inflammation-associated cancer[J]. Nature,2004,431(7007):461-466.
    [25]GONG D,SHI W,YI SJ,et al. TGF-βsignaling plays a critical role in promoting alternative macrophage activation[J]. BMC Immunology,2012,13(1):1-10.
    [26]Goswami K K,Barik S,Sarkar M,et al. Targeting STAT3phosphorylation by neem leaf glycoprotein prevents immune evasion exerted by supraglottic laryngeal tumor induced M2macrophages[J]. Molecular Immunology,2014,59(2):119-127.
    [27]Werno C,Menrad H,Weigert A,et al. Knockout of HIF-1αin tumor-associated macrophages enhances M2 polarization and attenuates their pro-angiogenic responses[J]. Carcinogenesis,2010,31(10):1863-1872.
    [28]ZHOU J,DING T,PAN W,et al. Increased intratumoral regulatory T cells are related to intratumoral macrophages and poor prognosis in hepatocellular carcinoma patients[J].International Journal of Cancer,2009,125(7):1640-1648.
    [29]Xing F,Saidou J,Watabe K,et al. Cancer associated fibroblasts(CAFS)in tumor microenvironment[J]. Front Biosci,2011,15(1):166-179.
    [30]Garin-Chesa P,Old L J,Rettig W J,et al. Cell surface glycoprotein of reactive stromal fibroblasts as a potential antibody target in human epithelial cancers[J]. Proc Natl Acad Sci USA,1990,87(18):7235-7239.
    [31]Wever O D,Mareel M. Role of tissue stroma in cancer invasion[J]. Journal of Pathology,2003,200(4):429-447.
    [32]Drake L E,Macleod K F. Tumour suppressor gene function in carcinoma-associated fibroblasts:from tumour cells via EMT and back again?[J]. Journal of Pathology,2014,232(3):283-288.
    [33]Mishra P J,Mishra P J,Humeniuk R,et al. Carcinomaassociated fibroblast-like differentiation of human mesenchymal stem cells[J]. Cancer Research,2008,68(11):4331-4339.
    [34]Potenta S,Zeisberg E,Kalluri R,et al. The role of endothelialto-mesenchymal transition in cancer progression[J]. British Journal of Cancer,2008,99(9):1375-1379.
    [35]Crisan M,Yap S,Casteilla L,et al. A perivascular origin for mesenchymal stem cells in multiple human organs[J]. Cell Stem Cell,2008,3(3):301-313.
    [36]Mueller M M,Fusenig N E. Friends or foes-bipolar effects of the tumour stroma in cancer[J]. Nature Reviews Cancer,2004,4(11):839-849.
    [37]Tlsty T D. Stromal cells can contribute oncogenic signals[J].Seminars in Cancer Biology,2001,11(2):97-104.
    [38]Elenbaas B,Weinberg R A. Heterotypic signaling between epithelial tumor cells and fibroblasts in carcinoma formation[J].Experimental Cell Research,2001,264(1):169.
    [39]董乔梅,李娟,赵丽,等. CXC趋化因子在肿瘤中的研究进展[J].西部医学,2013,25(4):639-640.
    [40]Benelli R,Stigliani S,Minghelli S,et al. Impact of CXCL1overexpression on growth and invasion of prostate cancer cell[J].Prostate,2013,73(9):941-951.
    [41]Frick V O,Rubie C,Wagner M,et al. Enhanced ENA-78 and IL-8 expression in patients with malignant pancreatic diseases[J]. Pancreatology,2008,8(4-5):488-497.
    [42]Bandapalli O R,Ehrmann F,Ehemann V,et al. Downregulation of CXCL1 inhibits tumor growth in colorectal liver metastasis[J]. Cytokine,2012,57(1):46-53.
    [43]DONG QM,ZHANG JQ,LI Q,et al. Clinical significance of serum expression of GROβin esophageal squamous cell carcinoma[J].World Journal of Gastroenterology,2011,17(21):2658.
    [44]Killian P H,Kronski E,Michalik K M,et al. Curcumin inhibits prostate cancer metastasis in vivo by targeting the inflammatory cytokines CXCL1 and-2[J]. Carcinogenesis,2012,33(12):2507-2519.
    [45]Kavandi L,Collier M A,Nguyen H,et al. Progesterone and calcitriol attenuate inflammatory cytokines CXCL1 and CXCL2in ovarian and endometrial cancer cells[J]. Journal of Cellular Biochemistry,2012,113(10):3143-3152.
    [46]BergersG,BrekkenR,McmahonG,etal.Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis[J]. Nature Cell Biology,2000,2(10):737.
    [47]DeryuginaEI,QuigleyJP.Pleiotropicrolesofmatrix metalloproteinasesintumorangiogenesis:Contrasting,overlapping and compensatory functions[J]. Biochimica Et Biophysica Acta Molecular Cell Research,2010,1803(1):103-120.
    [48]Masson V,Lr D L B,Munaut C,et al. Contribution of host MMP-2 and MMP-9 to promote tumor vascularization and invasion of malignant keratinocytes[J]. Faseb Journal,2005,19(2):234-236.
    [49]杨兰.中医正气学说探析[J].辽宁中医杂志,2004,31(2):113-114.
    [50]张慈安,魏品康,李勇进,等.痰浊与肿瘤微环境的相关性探讨[J]. Journal of Integrative Medicine,2010,8(3):215-219.
    [51]张葛,花宝金.从炎性微环境探究中医肿瘤病机与治则治法[J].中医杂志,2012,53(13):1101-1104.
    [52]熊露,田少霞.扶正培本治则方药调节肿瘤微环境免疫与血管正常化的思路研究[J].中国中西医结合杂志,2010,30(2):201-204.
    [53]李尧,钱文慧,陆茵,等.中医治则治法与肿瘤微环境[J].中医杂志,2011,22(21):1801-1804.
    [54]尤杰,刘嘉湘.刘嘉湘扶正治癌学术思想初探[J].中华中医药学刊,2011(8):1829-1831.
    [55]谢淮冰,房良华,王瑞平,等.健脾疏肝抗毒方对三阴性乳腺癌荷瘤鼠抗肿瘤作用的研究[J].时珍国医国药,2016(11):2637-2640.
    [56]李健,郝钰,张玉丽,等.小檗碱对CT26皮下移植瘤组织中肿瘤相关巨噬细胞的影响[J].中国组织化学与细胞化学杂志,2011,20(3):203-206.
    [57]邓珊,安红梅,胡兵,等.藤龙补中汤对大肠癌肺转移及肿瘤相关巨噬细胞作用[J].中国中西医结合消化杂志,2016(7):515-519.
    [58]张恩欣,周岱翰,侯超,等.益气除痰方抑制肿瘤相关巨噬细胞的抗肿瘤免疫功能研究[J].中华肿瘤防治杂志,2016,23(10):627-630.
    [59]包素珍,魏自太,李恒楠,等.加味黄芪建中汤对脾气虚证肺癌微环境肿瘤相关巨噬细胞表达的影响[J].浙江中医杂志,2017,52(6):438-439.
    [60]黎磊.扶正解毒方对小鼠前胃癌所诱导的肿瘤相关巨噬细胞干预作用研究[D].北京:北京中医药大学,2013.
    [61]Sica A,Larghi P,Mancino A,et al. Macrophage polarization in tumour progression[J]. Seminars in Cancer Biology,2008,18(5):349-355.
    [62]李柳叶,邢玉,包晓霞,等.白花蛇舌草黄酮和多糖对与肿瘤相关巨噬细胞共培养的人子宫内膜癌Ishikawa细胞的影响[J].中国妇产科临床杂志,2015(2):150-153.
    [63]司海龙,王立芳,徐振晔,等.肺岩宁颗粒对Lewis肺癌小鼠肿瘤相关巨噬细胞及肿瘤转移的影响[J].上海中医药大学学报,2016(3):47-52.
    [64]司海龙.基于肿瘤微环境探讨芪灵蟾调节肿瘤相关巨噬细胞的实验研究[D].上海:上海中医药大学,2016.
    [65]Chanmee T,Ontong P,Konno K,et al. Tumor-associated macrophages as major players in the tumor microenvironment[J].Cancers,2014,6(3):1670-1690.
    [66]宋卓.扶正解毒方对荷瘤小鼠肿瘤相关巨噬细胞介导下血管重塑的调控研究[D].北京:中国中医科学院,2016.
    [67]贾程辉.扶正解毒方对移植性前胃癌小鼠术后复发模型肿瘤相关巨噬细胞的调控作用研究[D].北京:北京中医药大学,2014.
    [68]黎金华,田菲,邱崇笙,等.扶正散结方调控Lewis肺癌小鼠TAMS免疫重塑作用的相关研究[J].中国中药杂志,2015,40(6):1161-1165.
    [69]李枋霏.扶正解毒方对体外诱导型肿瘤相关巨噬细胞的干预调控作用研究[D].北京:中国中医科学院,2014.
    [70]阮善明,沈敏鹤,林红,等.解毒三根汤干预肿瘤相关成纤维细胞及抑制结肠癌侵袭转移的实验研究[J].中国中西医结合杂志,2013,33(9):1242-1246.
    [71]陈联誉.微环境中肿瘤相关成纤维细胞介导的清热化湿中药抗胰腺癌作用研究[D].上海:复旦大学,2013
    [72]郝钦,杨永雁,韩雅玲,等.漏芦逆转胃癌相关成纤维细胞促癌作用的研究[J].中药药理与临床,2017(1):119-123.
    [73]张齐.黄芪多糖对肺癌细胞共培养体系中BMSCs增殖规律及TAFs相关分子表达的影响[D].兰州:甘肃中医药大学,2015.
    [74]武有明,张齐,刘永琦,等.当归多糖对肺癌微环境中骨髓间充质干细胞增殖及TAFs相关分子表达的影响[J].中国细胞生物学学报,2015(9):1271-1277.