吉林大学学报(医学版) ›› 2022, Vol. 48 ›› Issue (1): 265-270.doi: 10.13481/j.1671-587X.20220134
• 综述 • 上一篇
收稿日期:2021-01-27
出版日期:2022-01-28
发布日期:2022-01-17
通讯作者:
赵丽艳
E-mail:970201043@qq.com
作者简介:李 峣(1997-),女,山东省诸城县人,在读硕士研究生,主要从事胶质瘤发病机制方面的研究。
基金资助:
Received:2021-01-27
Online:2022-01-28
Published:2022-01-17
摘要:
血小板源性生长因子D(PDGF-D)是血小板源性生长因子(PDGFs)家族中新近被发现的成员,具有特殊的生物学功能。PDGF-D在包括胶质瘤在内的多种肿瘤组织中呈高表达,并能促进肿瘤细胞上皮-间质转化(EMT)过程。胶质瘤具有侵袭性生长的特性,该特性与EMT有密切关联。Notch1是Notch家族成员之一,参与肿瘤细胞的EMT过程,在PDGF-D促进肿瘤的生长和迁移过程中扮演重要角色。PDGF-D可能通过Notch1信号通路在包括胶质瘤在内的肿瘤细胞EMT过程中发挥效应。现对PDGF-D促进肿瘤细胞EMT、特别是对胶质瘤细胞EMT的调控作用及Notch1信号通路在该过程的可能作用进行简要综述。
中图分类号:
李峣,孙莹,宋燕珂,汪敏,贾茗博,赵丽艳. PDGF-D通过Notch1信号通路对肿瘤细胞上皮-间质转化调控作用的研究进展Research progress in regulatory effect of PDGF-D on epithelial-mesenchymal transition in tumor cells through Notch1 signaling pathway[J]. 吉林大学学报(医学版), 2022, 48(1): 265-270.
| 1 | 贾茗博, 孙 莹, 赵丽艳. 血小板源生长因子在肿瘤侵袭、转移和上皮间质转化中作用的研究进展[J]. 中国实验诊断学, 2019, 23(6): 1103-1107. |
| 2 | 颉晚林, 邹 磊, 孙轶华. PDGF-D及其相关信号传导通路在肿瘤发生发展中的作用[J]. 实用癌症杂志, 2019, 34(5): 868-870. |
| 3 | 钱丁丁, 周建庆. PDGF-C和PDGF-D对心血管系统疾病影响的研究进展[J]. 浙江医学, 2019, 41(22): 2440-2443. |
| 4 | CHEN J, YUAN W, WU L, et al. PDGF-D promotes cell growth, aggressiveness, angiogenesis and EMT transformation of colorectal cancer by activation of Notch1/Twist1 pathway[J]. Oncotarget, 2017, 8(6): 9961-9973. |
| 5 | ZHANG H, SUN J D, YAN L J, et al. PDGF-D/PDGFRβ promotes tongue squamous carcinoma cell (TSCC) progression via activating p38/AKT/ERK/EMT signal pathway[J]. Biochem Biophys Res Commun, 2016, 478(2): 845-851. |
| 6 | DEVARAJAN E, SONG Y H, KRISHNAPPA S,et al. Epithelial-mesenchymal transition in breast cancer lines is mediated through PDGF-D released by tissue-resident stem cells[J]. Int J Cancer, 2012, 131(5): 1023-1031. |
| 7 | KIM M S, CHOI H S, WU M X, et al. Potential role of PDGFRβ-associated THBS4 in colorectal cancer development[J]. Cancers, 2020, 12(9): 2533. |
| 8 | WANG Z, LI Y, KONG D, et al. The role of Notch signaling pathway in epithelial-mesenchymal transition (EMT) during development and tumor aggressiveness[J]. Curr Drug Targets, 2010, 11(6): 745-751. |
| 9 | 杨 允, 戴 德. PDGF-D在肿瘤生长及肿瘤靶向VEGF治疗中的研究现状[J]. 海南医学,2014, 25(20): 3042-3044. |
| 10 | REIGSTAD L J, VARHAUG J E, LILLEHAUG J R. Structural and functional specificities of PDGF-C and PDGF-D, the novel members of the platelet-derived growth factors family[J]. FEBS J, 2005, 272(22): 5723-5741. |
| 11 | USTACH C V, KIM H R. Platelet-derived growth factor D is activated by urokinase plasminogen activator in prostate carcinoma cells[J].Mol Cell Biol,2005,25(14): 6279-6288. |
| 12 | HELDIN C H, ERIKSSON U, OSTMAN A. New members of the platelet-derived growth factor family of mitogens[J].Arch Biochem Biophys, 2002, 398(2): 284-290. |
| 13 | ROSKOSKI R. The role of small molecule platelet-derived growth factor receptor (PDGFR) inhibitors in the treatment of neoplastic disorders[J]. Pharmacol Res, 2018, 129: 65-83. |
| 14 | NAJY A J, JUNG Y S, WON J J, et al. Cediranib inhibits both the intraosseous growth of PDGF-D positive prostate cancer cells and the associated bone reaction[J]. Prostate, 2012, 72(12): 1328-1338. |
| 15 | NORDBY Y, RICHARDSEN E, RAKAEE M, et al. High expression of PDGFR-β in prostate cancer stroma is independently associated with clinical and biochemical prostate cancer recurrence[J]. Sci Rep, 2017, 7: 43378. |
| 16 | LI H, FREDRIKSSON L, LI X, et al. PDGF-D is a potent transforming and angiogenic growth factor[J]. Oncogene, 2003, 22(10): 1501-1510. |
| 17 | KESARI S. Understanding glioblastoma tumor biology: the potential to improve current diagnosis and treatments[J]. Semin Oncol, 2011, 38: S2-S10. |
| 18 | COLELLA B, FAIENZA F, DI BARTOLOMEO S. EMT regulation by autophagy: a new perspective in glioblastoma biology[J]. Cancers(Basel), 2019,11(3):312. |
| 19 | SHIH A H, HOLLAND E C. Platelet-derived growth factor (PDGF) and glial tumorigenesis[J]. Cancer Lett, 2006, 232(2): 139-147. |
| 20 | LOKKER N A, SULLIVAN C M, HOLLENBACH S J,et al. Platelet-derived growth factor (PDGF) autocrine signaling regulates survival and mitogenic pathways in glioblastoma cells: evidence that the novel PDGF-C and PDGF-D ligands may play a role in the development of brain tumors[J]. Cancer Res, 2002, 62(13): 3729-3735. |
| 21 | GONDI C S, VEERAVALLI K K, GORANTLA B, et al. Human umbilical cord blood stem cells show PDGF-D-dependent glioma cell tropism in vitro and in vivo [J]. Neuro Oncol, 2010, 12(5): 453-465. |
| 22 | THIERY J P, ACLOQUE H, HUANG R Y, et al. Epithelial-mesenchymal transitions in development and disease[J]. Cell, 2009, 139(5): 871-890. |
| 23 | 侯 鑫. PDGF-D通过EMT参与吉西他滨在肝细胞癌中的耐药机制研究[D]. 蚌埠: 蚌埠医学院, 2014. |
| 24 | AHMED N, MAINES-BANDIERA S, QUINN M A, et al. Molecular pathways regulating EGF-induced epithelio-mesenchymal transition in human ovarian surface epithelium[J]. Am J Physiol Cell Physiol, 2006, 290(6): C1532-C1542. |
| 25 | GOTZMANN J, FISCHER A N, ZOJER M, et al. A crucial function of PDGF in TGF-beta-mediated cancer progression of hepatocytes[J]. Oncogene, 2006, 25(22): 3170-3185. |
| 26 | STRUTZ F, ZEISBERG M, ZIYADEH F N, et al. Role of basic fibroblast growth factor-2 in epithelial-mesenchymal transformation[J]. Kidney Int, 2002, 61(5): 1714-1728. |
| 27 | YANG L, LIN C, LIU Z R. P68 RNA helicase mediates PDGF-induced epithelial mesenchymal transition by displacing Axin from beta-catenin[J]. Cell, 2006, 127(1): 139-155. |
| 28 | 王永娟,谢肖立,姜慧卿,等.肝纤维化中上皮间质转化的调控及靶向治疗的研究进展[J]. 临床肝胆病杂志,2021,37(1): 165-168. |
| 29 | DU C, ZHANG C, HASSAN S, et al. Protein kinase D1 suppresses epithelial-to-mesenchymal transition through phosphorylation of snail[J]. Cancer Res, 2010, 70(20): 7810-7819. |
| 30 | SON H, MOON A. Epithelial-mesenchymal transition and cell invasion[J]. Toxicol Res,2010,26(4): 245-252. |
| 31 | GHELDOF A, BERX G. Cadherins and epithelial-to-mesenchymal transition[J]. Prog Mol Biol Transl Sci, 2013, 116: 317-336. |
| 32 | KAHLERT U D, MACIACZYK D, DOOSTKAM S, et al. Activation of canonical WNT/β-catenin signaling enhances in vitro motility of glioblastoma cells by activation of ZEB1 and other activators of epithelial-to-mesenchymal transition[J]. Cancer Lett, 2012,325(1): 42-53. |
| 33 | IWADATE Y. Epithelial-mesenchymal transition in glioblastoma progression[J]. Oncol Lett, 2016, 11(3): 1615-1620. |
| 34 | ISER I C, PEREIRA M B, LENZ G, et al. The epithelial-to-mesenchymal transition-like process in glioblastoma: an updated systematic review and in silico investigation[J]. Med Res Rev, 2017, 37(2): 271-313. |
| 35 | SINGH S K, CLARKE I D, TERASAKI M, et al. Identification of a cancer stem cell in human brain tumors[J]. Cancer Res, 2003, 63(18): 5821-5828. |
| 36 | CARRO M S, LIM W K, ALVAREZ M J, et al. The transcriptional network for mesenchymal transformation of brain tumours[J]. Nature, 2010,463(7279):318-325. |
| 37 | KONG D, WANG Z, SARKAR S H, et al. Platelet-derived growth factor-D overexpression contributes to epithelial-mesenchymal transition of PC3 prostate cancer cells[J]. Stem Cells, 2008, 26(6): 1425-1435. |
| 38 | MIELE L, MIAO H, NICKOLOFF B J. NOTCH signaling as a novel cancer therapeutic target[J]. Curr Cancer Drug Targets, 2006, 6(4): 313-323. |
| 39 | RANGANATHAN P, WEAVER K L, CAPOBIANCO A J. Notch signalling in solid tumours: a little bit of everything but not all the time[J]. Nat Rev Cancer, 2011, 11(5): 338-351. |
| 40 | 王闻楚. E-cadherin通过Notch信号通路介导前列腺癌耐药的分子机制[D]. 南宁: 广西医科大学, 2015. |
| 41 | YI L, ZHOU X, LI T, et al. Notch1 signaling pathway promotes invasion, self-renewal and growth of glioma initiating cells via modulating chemokine system CXCL12/CXCR4[J]. J Exp Clin Cancer Res,2019,38(1): 339. |
| 42 | JIANG L G, WU J, CHEN Q H, et al. Notch1 expression is upregulated in glioma and is associated with tumor progression[J]. J Clin Neurosci, 2011, 18(3): 387-390. |
| 43 | LEONG K G, NIESSEN K, KULIC I, et al. Jagged1-mediated Notch activation induces epithelial-to-mesenchymal transition through Slug-induced repression of E-cadherin[J]. J Exp Med, 2007, 204(12): 2935-2948. |
| 44 | 游 焜,王大军,王 亮,等. 敲除NOR1基因对人肝癌裸鼠移植瘤的影响及作用机制[J]. 临床肝胆病杂志,2020,36(2): 381-386. |
| 45 | BILLOTTET C, TUEFFERD M, GENTIEN D, et al. Modulation of several waves of gene expression during FGF-1 induced epithelial-mesenchymal transition of carcinoma cells[J]. J Cell Biochem, 2008, 104(3): 826-839. |
| 46 | TIMMERMAN L A, GREGO-BESSA J, RAYA A, et al. Notch promotes epithelial-mesenchymal transition during cardiac development and oncogenic transformation[J]. Genes Dev, 2004, 18(1): 99-115. |
| 47 | SAHLGREN C, GUSTAFSSON M V, JIN S, et al. Notch signaling mediates hypoxia-induced tumor cell migration and invasion[J]. PNAS, 2008, 105(17): 6392-6397. |
| 48 | NIESSEN K, FU Y, CHANG L, et al. Slug is a direct Notch target required for initiation of cardiac cushion cellularization[J]. J Cell Biol, 2008, 182(2): 315-325. |
| 49 | LI J L, LI Q B, LIN L, et al. Targeting the Notch1 oncogene by miR-139-5p inhibits glioma metastasis and epithelial-mesenchymal transition (EMT)[J]. BMC Neurol, 2018, 18(1): 133. |
| 50 | 赵 林, 张才全, 廖 刚, 等. PDGF-D和VEGF在胃癌中的表达及其意义[J].基础医学与临床,2009,29(12): 1305-1309. |
| 51 | HUANG H. Matrix metalloproteinase-9 (MMP-9) as a cancer biomarker and MMP-9 biosensors: recent advances[J]. Sensors (Basel),2018, 18(10):3249. |
| [1] | 任俏同,吴维华,王星翔,王世超,程一鹏,历春. 沉默白细胞介素17 受体B基因对肺腺癌A549细胞增殖、侵袭和凋亡的影响及其机制[J]. 吉林大学学报(医学版), 2026, 52(3): 738-745. |
| [2] | 张丽娜,孟哲思,巴隆,孟峻. 细胞分裂周期蛋白6与肿瘤发生发展关系的研究进展[J]. 吉林大学学报(医学版), 2026, 52(3): 847-853. |
| [3] | 朱平胜,葛思堂,左芦根,陈德利,张洋洋. miR-325-3p靶向PRELID1基因介导EMT通路对结肠癌细胞侵袭和迁移的影响及其机制[J]. 吉林大学学报(医学版), 2025, 51(5): 1185-1193. |
| [4] | 沈维高,刘雨齐,张骏,林珈羽,崔航,刘艳波. 白细胞介素33对恶性脑胶质瘤发生发展影响的生物信息学分析及其实验验证[J]. 吉林大学学报(医学版), 2025, 51(5): 1318-1332. |
| [5] | 沈忠军,赵钥,贾茗博,赵丽艳. 缺氧诱导因子在胶质瘤细胞上皮-间质转化过程中对细胞迁移和侵袭影响的研究进展[J]. 吉林大学学报(医学版), 2025, 51(4): 1145-1154. |
| [6] | 王星翔,赵颖,任俏同,王鹤霏,蒲刚,历春. M2巨噬细胞通过调控NF-κB信号通路对非小细胞肺癌A549细胞上皮-间质转化和顺铂耐药的促进作用[J]. 吉林大学学报(医学版), 2025, 51(3): 642-652. |
| [7] | 刘东慧,次云哲,王春艳,麻雯熠. miR-199a-5p对胶质瘤U251细胞小窝蛋白1表达及细胞迁移和凋亡的影响[J]. 吉林大学学报(医学版), 2025, 51(3): 663-671. |
| [8] | 王繁,温馨,王艺璇,王远. 缝隙连接蛋白β2对肺腺癌患者预后及肺腺癌A549细胞生物学行为的影响[J]. 吉林大学学报(医学版), 2025, 51(3): 716-726. |
| [9] | 王妍,赵邹宇,于盼盼,杨萍. IκB激酶相互作用蛋白在宫颈癌组织中的表达及其对宫颈癌细胞增殖、迁移和侵袭的影响[J]. 吉林大学学报(医学版), 2025, 51(2): 341-351. |
| [10] | 王飞娜,米旭光,林秀英,付建华,刘磊,于歆悦,臧欢欢,刘霖君,陈士玲,方艳秋. Wnt/β-catenin信号通路抑制剂MSAB对人子宫内膜基质细胞纤维化反应的影响[J]. 吉林大学学报(医学版), 2024, 50(5): 1266-1274. |
| [11] | 刘洋,刘志,孙可,金嘉慧,任俊. LGI-1抗体阳性自身免疫性脑炎伴睡眠结构异常和认知障碍1例报告及文献复习[J]. 吉林大学学报(医学版), 2024, 50(4): 1137-1143. |
| [12] | 梁超,代娟娟,周宁,王丹丹,赵杰,安迪,武艳. 冬凌草甲素对人鼻咽癌HONE-1细胞增殖、迁移和凋亡的影响[J]. 吉林大学学报(医学版), 2024, 50(4): 917-924. |
| [13] | 高世磊,王家强,姚伟涛,田志超,李超,梁潇潇,王鑫. miR-761通过调控肿瘤相关巨噬细胞极化对骨肉瘤MG63细胞上皮-间质转化的影响[J]. 吉林大学学报(医学版), 2024, 50(4): 978-988. |
| [14] | 魏海峰,倪志强,魏雁虹,王起来,李首庆,马寅芙,谭岩,方艳秋. miR-126过表达和ADAM9基因沉默对胃癌SGC-7901细胞生物学行为的影响及其机制[J]. 吉林大学学报(医学版), 2024, 50(2): 310-319. |
| [15] | 那佈其,权春姬,赵芳,杨凡,肖茹,金雪梅,李珍玲. 组蛋白去乙酰化酶抑制剂CUDC-101对前列腺癌DU145细胞DNA损伤、迁移和上皮-间质转化的影响[J]. 吉林大学学报(医学版), 2024, 50(2): 400-410. |
|
