期刊文献+

舌鳞状细胞癌中肿瘤干细胞耐药性研究 被引量:2

Chemotherapy-resistance of Cancer Stem Cells in Squamous Cell Cacinoma of Tongue
下载PDF
导出
摘要 目的:探讨舌鳞状细胞癌中肿瘤干细胞对化疗的耐受作用。方法:用磁珠分选技术、细胞免疫荧光染色和药物毒性试验等方法,研究经分选后得到的肿瘤干细胞和阴性细胞在化疗药物作用后其细胞增殖活性的差异。结果:细胞免疫荧光结果显示,CD133和CD44在分选出来的CD133+/CD44+细胞高表达而在CD133-/CD44-细胞基本不表达。CCK8实验结果显示分选出来的CD133+/CD44+细胞较CD133-/CD44-细胞在化疗药物作用下有更高的细胞成活率。结论:经磁珠分选出来的舌癌肿瘤干细胞(CD133+/CD44+细胞)更能耐受化疗药物的作用。 Objective: To investigate the chemotherapy-resistance of cancer stem cells in squamous cell cacinoma of tongue. Methods: CD133^+/CD44^+ and CD133^-/CD44^- subpopulation cells were sorted by magnetic cell sorting (MACS). Single isolated CD133^+/CD44^+ and CD133-/CD44-cells were cultured in RPMI-1640 medium,containing basic fibroblast growth factor (bFGF, 10ng/mL),epidermal growth factor (EGF, 20ng/mL). Immunofluo- rescence was applied to detect the expression of CD133 and CD44 in these two subpopulation cells. CCK-8 assay was performed to analyze the drug sensitivity of the two subpopulation to anti-tumor drug,Cisplatin, 5-Fluoroura- cil and Vincristine. Result: Cell immunofluorescence showed that CD133 and CD44 could be detected in CD133^+/ CD44^+ cells while they could not be detected in CD133^-/CD44^- cells. Chemotherapeutic agents had a more obvious inhibitory effect on CD133^-/CD44^- cells than CD133^+/CD44^+ cells. Conclusion: The cancer stem cells in squamous cell cacinoma of tongue(CD133^+/CD44^+ cells) that sorted by MACS showed strong capability of tumor's re sistance to chemotherapeutic agents than CD133^-/CD44^- cells.
出处 《口腔医学研究》 CAS CSCD 2012年第1期1-4,8,共5页 Journal of Oral Science Research
基金 国家自然科学基金项目(编号:81000679) 中央高校基本科研业务费专项资金资助(3082026)
关键词 肿瘤 鳞状细胞 肿瘤干细胞 化疗抑制 Neoplasms Squamous cell Neoplastic stem cells Chemotherapy-resistance
  • 相关文献

参考文献16

  • 1陈坤,习利军,姜倩,张铁柱,于立明,凌瑞,谢镇春.CD44V6、MMP-9在舌癌中的表达及其意义[J].口腔医学研究,2010,26(5):740-743. 被引量:8
  • 2Dalerba P, Cho RW, Clarke MF. Cancer Stem Cells:Models and Conceptsp [J]. Annu. Rev. Med, 2007, 58: 267-284. 被引量:1
  • 3Ai--Hajj M, Wicha MS, Benito--Hernandez A, et al. Pro- spective identification of tumorigenic breast cancer cells[J]. Proc. Natl Acad. Sci, 2003(100) : 3983--3988. 被引量:1
  • 4Singh SK, Hawkins C, Clarke ID, et al. Identification of hu- man brain tumoor initiating cells [J]. Nature, 2004 (432) : 396--401. 被引量:1
  • 5O'Brien CA, Pollett A, Gallinger S, et al. A human colon cancer cell capable of initiating turnout growth in immunodefi- cient mice[J]. Nature, 2007(445) : 106--110. 被引量:1
  • 6Hermann PC, Huber Sir, Herrler T, et al. Distinct popula- tions of cancer stem cells determine tumor growth and meta- static activity in human pancreatic cancer [J]. Cell Stem Cell, 2007(1) : 313--323. 被引量:1
  • 7Eramo A, Lotti F, Sette G, et al. Identification and expansion of the tumorigenic lung cancer stem cell population [J]. Cell Death Differ, 2008(15) : 504--514. 被引量:1
  • 8Yang ZF, Ho DW, Ng MN, et al. Significance of CD90+ cancer stem cells in human liver cancer [J]. Cancer Cell, 2008 (13) : 153--166. 被引量:1
  • 9Schatton T, Murphy GF, Fank NY, et al. Identification of cells initiating human melanomas [J]. Nature, 2008(451) : 345--349. 被引量:1
  • 10Visvader JE, Lindeman GJ. Cancer stem cells in solid tumours accumulati,ng evidence and unresolved questions [J]. Nature reviews cancer, 2008(8) : 755--768. 被引量:1

二级参考文献13

  • 1Wong YF, Cheung TH, Tsao GS. Genome--wide gene expression profiling of cervical cancer in Hong Kong women by oligonucleotide microarray [J]. Int J Cancer, 2006, 118(10) : 2461-2469. 被引量:1
  • 2Cha HJ, Bae SK, Lee, HY, et al. Anti--invasive aetivity of ursolic acid correlates with the reduced expressor of matrix metal proteinaseg (MMP--9) in HT-1080 human fibrosarcoma cells [J]. Cancer Res, 1996, 56(10) : 2281-2284. 被引量:1
  • 3Nguyen VN, Mireiovsky T, Melinova L, et al. CD44 and its v6 spiliced variant in lung carcinoma relation toNCAM, CEA,EMA and UP1 and prognostic significance [J].Neoplasma, 2004, 47(6): 400--408. 被引量:1
  • 4Rautava J, Soukka T, Inki P, et al. CD44v6 in developing, dysplastic and malignant oral epithelia[J]. Oral Oncol, 2003, 39(4) : 373-379. 被引量:1
  • 5Cruz MC, Pereira AL, Lopes FF, et al. Immunohistochemical expression of E--cadherin and CD44V6 in squamous cell carcinomas of the lower lip and tongue [J]. Braz Dent J, 2009, 20(1) : 64--69. 被引量:1
  • 6Guler G, Sarac s, Uner A, et al. Prognostic value of CD44V6 in laryngeal epidermoid carcinomas [J]. Arch Otolaryngol Head Neck Surg, 2002, 128(4) : 393-397. 被引量:1
  • 7Bhuvarahamurthy V, Kristiansen GO, Johannsen M, et al. In situ gene expression and localization of metalloproteinases MMP1, MMP2, MMP3, MMPg, and their inhibitors TIMP1 and TIMP2 in human renal cell carcinoma [R]. Oncol Rep, 2006, 15(5) :1379-1384. 被引量:1
  • 8Wickramasinghe NS, Nagaraj NS, Vigneswaran N, et al. Catheps in B promotes both motility and invasiveness of oral carcinoma cells [J]. Arch Biochem Biophys, 2005, 436(1) : 187-195. 被引量:1
  • 9Sato S, Miyauchi M, Ogawa I, et al. Inhibition of CD44V9 upregulates the invasion ability of oral squamous ceil carcinoma cells []]. Oral Oncol, 2003, 39(1) : 27-30. 被引量:1
  • 10Yu Q, Stamenkovic I. Localization of matrix metalloprotein- ase 9 to the cell surface provides a mechanism for CD44--mediated tumor invasion [J]. Gengs Dev, 1999, 13(1) : 35-- 48. 被引量:1

共引文献7

同被引文献14

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部