期刊文献+

EP4受体拮抗剂对雄激素非依赖性前列腺癌PC3细胞恶性表型的影响 被引量:1

Effect of EP4 receptor antagonist on malignant phenotypes of androgen-independent prostate cancer cells PC3
原文传递
导出
摘要 目的探讨EP4受体拮抗剂ONO-AE3-208对雄激素非依赖性前列腺癌(AIPC)PC3细胞的体外抗肿瘤效应。方法采用RT-PCR检测EP4受体mRNA在PC3细胞中的表达水平,实验组以0.1、1和10μmol/L的ONO-AE3-208作用于PC3细胞,对照组加入同体积的超轻水(ODW),采用MTT比色法、划痕愈合实验和细胞侵袭实验观察ONO-AE3-208对前列腺癌PC3细胞增殖、迁移和侵袭能力的抑制效应。结果 EP4受体在PC3细胞中呈高水平表达;随ONO-AE3-208作用时间和浓度的增加,其对PC3细胞的抑制率没有变化。PC3细胞的实验组细胞迁移比例为(25.30±6.11)%,低于对照组的(40.18±7.25)%(P<0.05)。实验组用0.1、1和10μmol/L的ONO-AE3-208作用于PC3细胞24h后,其穿入下室细胞数分别为(19.72±3.39)、(15.61±3.11)和(10.39±2.15)个/视野,少于对照组的(24.67±3.75)个/视野(P<0.05)。结论 EP4受体在AIPC PC3细胞中表达明显升高。EP4受体拮抗剂ONO-AE3-208对AIPC PC3细胞的增殖没有影响,但对其迁移和侵袭能力有明显的抑制作用。 Objective To investigate the anti-tumor effect of EP4 receptor antagonist ONO- AE3-208 on androgen-independent prostate cancer(AIPC) cells PC3 in vitro. Methods Quantative RT-PCR was used to examine the EP4 mRNA expression in the PC3 cells. The influenee of ONO- AE3-208 on the proliferation of the cells was observed by MTT assay. Wound-healing assay and Transwell invasion assay were used to evaluate the inhibitory effect of ONO-AE3-208 on the ability of migration and invasion- Results EP4 was highly expressed in cell lines PC3. As the time and concentration inereased,EP4 antagonist ONO-AE3-208 did not influence the proliferation of the cells (P〉0. 05). The migration distance ratio of ONO-AF.3-208 10 μmol/L in treatment group was (25. 30±6. ll)%,which was lower than (40. 18±7.25)% in control group(P〈0. 05). After treated with ONO-AE3-208 0. 1,1.0 and10 μmol/L for 24 hours,the numbers of PC3 cells were (19.72±3. 39), (15.61±3. 11) and (10.39±2.15) pieces/view,which were more than (24. 67±3.75) pieces/view in control group(P〈0. 05). Conclusion AIPC PC3 cells highly express EP4. EP4 antagonist ONO-AE3- 208 does not effect the proliferation of AIPC PC3, but can suppress its ability of migration and invasion.
出处 《江苏医药》 CAS 北大核心 2014年第5期497-500,F0002,共5页 Jiangsu Medical Journal
基金 国家自然科学基金(81372742)
关键词 EP4受体 前列腺癌 EP4 receptor Prostate cancer
  • 相关文献

参考文献12

  • 1Smith MR, Manola J, Kaufman DS, et al. Celecoxib versus placebo for men with prostate cancer and a rising serttrn prostate-specific antigen after radical prostatectomy and/or radiation therapy[J-]. J Clin Oncol, 2006,24 (18) : 2723-2728.
  • 2Terada N, Shimizu Y,Kamba T, et al. Identification of EP4 asa potential target for the treatment of castration-resistant prostate cancer using a novel xenograft model EJ. Cancer Res, 2010,70(4) : 1606-1615.
  • 3Gupta S, Srivastava M, Abroad N, et al. Over-expression of cyclooxygenase-2 in human prostate adenocarcinoma [-J "]. Prostate, 2000,42 (1) : 73-78.
  • 4Chen Y, Hughes-Fulford M. Prostaglandin E2 and the protein kinase A pathway mediate arachidonic acid induction of c-los in human prostate cancer cellsEJ. Br J Cancer, 2000, 82(12) .. 2000-2006.
  • 5许松,周文泉,张征宇,葛京平,高建平.选择性环氧化酶2抑制剂塞来昔布对人前列腺癌PC-3细胞增殖与凋亡的影响[J].中华男科学杂志,2008,14(6):489-493. 被引量:7
  • 6Kuo KT, Wang HW, Chou TY, et al. Prognostic role of PGE2 receptor EP2 in esophageal squamous cell carcinoma [J]. Ann Surg Oneol, 2009,16(2) : 352-360.
  • 7Rohertson FM, Simeone AM, Lucei A, et al. Differential regulation of the aggressive phenotype of inflammatory breast cancer cells by prostanoid receptors EP3 and EP4 [J]. Cancer,2010,116(11 Suppl) :2806-2814.
  • 8Risbridger GP,Davis ID, Birrell SN,et al. Breast and prostate cancer:more similar than different EJ]- Nat Rev Cancer, 2010,10(3) :205-212.
  • 9Ma X, Holt D, Kundu N, et al. A prostaglandin E (PGE) receptor EP4 antagonist protects natural killer cells from PGE ( 2 )-mediated and inhibits breast cancer metastasisJ']. Oncoimmunology, 2013,2 (1) : e22647.
  • 10Dong Z, Bonfil RD, Chinni S, et al. Matrix metalloproteinase activity and osteoelasts in experimental prostate cancer bone metastasis tissueEJ]. AmJ Pathol,2005,166(4):l173-1186.

二级参考文献8

  • 1丁翔,严春寅,温端改,侯建全,浦金贤.COX-2、bcl-2和PCNA在前列腺癌中的表达及其意义[J].苏州大学学报(医学版),2005,25(1):110-112. 被引量:10
  • 2Liu XH, Kirschenhaum A, Lu A, et al stimulates prostatic intraepithelial neoplasia Prostaglandin E ( 2 ) cell growth through activation of the interleukin-6/GP130/STAT-3 signaling pathway [J]. Biochem Biophys Res Commun, 2002, 290( 1 ) : 249-255.
  • 3Shahedi K, Lindstrom S, Zheng SL, et al. Genetic variation in the COX-2 gene and the association with prostate cancer risk [ J ]. Int J Cancer, 2006, 119 (3) :668-672.
  • 4Hussain T, Gupta S, Mukhtar H. Cyclooxygenase-2 and prostate carcinogenesis[J]. Cancer Lett, 2003, 191(2): 125-135.
  • 5Narayanan BA, Reddy BS, Bosland MC, et al. Exisulind in combination with celecoxib modulates epidermal growth factor receptor, cyclooxygenase-2, and cyclin D1 against prostate carcinogenesis: in vivo evidence[J]. Clin Cancer Res, 2007, 13(19) : 5965 -5973.
  • 6Smith MR, Manola J, Kaufman DS,et al. Celecoxib versus placebo for men with prostate cancer and a rising serum prostate-specific antigen after radical prostatectomy and/or radiation therapy [J]. JClinOncol, 2006, 24(18) :2723-2728.
  • 7Pruthi RS, Derksen JE, Moore D,et al. Phase Ⅱ trial of celecoxib in prostate-speeific antigen recurrent prostate cancer after definitive radiation therapy or radical prostatectomy[ J]. Clin Cancer Res, 2006, 12(7 Pt 1 ) :2172-2177.
  • 8Caries J, Font A, Mellado B, et al. Weekly administration of docetaxel in combination with estramustine and eelecoxib in patients with advanced hormone-refractory prostate cancer: final results fromaphase Ⅱ study[J]. Br J Cancer, 2007, 97(9): 1206- 1210.

共引文献6

同被引文献15

  • 1Hess KR, terns in ad Varadhachary GR, Taylor SH, et al. Metastatic pat- Cancer, 2006, 106(7) : 1624-1633.
  • 2Weinfurt KP, Li Y, Castel LD, et al. The significance of skele- tal-related events for the health-related quality of life of patients with metastatic prostate cancer. Ann Oneol, 2005,16 (4) : 579- 584.
  • 3Gupta S, Adhami VM, Subbarayan M, et al. Suppression of prostate carcinogenesis by dietary supplementation of celecoxib in trausgenic adenocarcinoma of the mouse prostate model. Cancer Res, 2004, 64(9) : 3334-3343.
  • 4Ray WA, Stein CM, Daugherty JR, et al. COX-2 selective non- steroidal anti-inflammatory drugs and risk of serious coronary heart disease. Lancet, 2002, 360(9339) : 1071-1073.
  • 5Xu S, Zhang Z, Ogawa O, et al. An EP4 antagonist ONO-AE3- 208 suppresses cell invasion, migration, and metastasis of pros- tate cancer. Cell Biochem Biophys, 2014 Apr 18.
  • 6Kundu N, Ma X, Kochel T, et al. Prostaglandin E receptor EP4 is a therapeutic target in breast cancer cells with stem-like proper- ties. Breast Cancer Res Treat, 2014, 143(1 ) : 19-31.
  • 7Ma X, Holt D, Kundu N, et al. A prostaglandin E (PGE) re- ceptor EP4 antagonist protects natural killer cells from PGE (2)- mediated immunosuppression and inhibits breast cancer metasta- sis. Oncoimmunology, 2013, 2(1 ) : e22647.
  • 8Ye L, Kynaston HG, Jiang WG. Bone metastasis in prostate cancer: Molecular and cellular mechanisms (Review). Int J Mol Med, 2007, 20(1) : 103-111.
  • 9Rentsch CA, Cecchini MG, Thalmann GN. Loss of inhibition over master pathways of bone mass regulation results in osteoscle- rotic bone metastases in prostate cancer. Swiss Med Wkly, 2009, 139(15-16) : 220-225.
  • 10Shamir D, Keila S, Weinreb M. A selective EP4 receptor anta- gonist abrogates the stimulation of osteoblast recruitment from bone marrow stromal cells by prostaglandin E2 in vivo and in vitro. Bone, 2004. 34(1) : 157-162.

引证文献1

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