国际检验医学杂志
國際檢驗醫學雜誌
국제검험의학잡지
INTERNATIONAL JOURNAL OF LABORATORY MEDICINE
2014年
14期
1880-1881,1884
,共3页
腹腔%卵巢上皮性癌%转移
腹腔%卵巢上皮性癌%轉移
복강%란소상피성암%전이
enterocoelia%epithelial ovarian cancer%metastasis
目的:探讨腹腔微环境与卵巢上皮性癌腹腔转移关系的研究。方法采用 RT-PCR 法及免疫组化法检测卵巢上皮性癌组织相应趋化因子受体及其配体的表达情况,腹膜组织相应配体的表达情况,以揭示趋化因子介导上皮性卵巢癌腹腔内转移机制。结果趋化因子受体 CXCR4在卵巢上皮性癌组织中表达明显高于其他趋化因子受体表达(P <0.01);趋化因子受体 CX-CR4的配体 SDF-1在上皮性卵巢癌组织和腹膜中均高表达。结论趋化因子 SDF-1及其受体 CXCR4在卵巢癌组织中高表达,通过自分泌作用,可能刺激卵巢癌细胞的过度生长;SDF-1在腹膜组织高表达,通过旁分泌作用,可能介导表达 CXCR4的卵巢癌细胞向腹腔内转移。
目的:探討腹腔微環境與卵巢上皮性癌腹腔轉移關繫的研究。方法採用 RT-PCR 法及免疫組化法檢測卵巢上皮性癌組織相應趨化因子受體及其配體的錶達情況,腹膜組織相應配體的錶達情況,以揭示趨化因子介導上皮性卵巢癌腹腔內轉移機製。結果趨化因子受體 CXCR4在卵巢上皮性癌組織中錶達明顯高于其他趨化因子受體錶達(P <0.01);趨化因子受體 CX-CR4的配體 SDF-1在上皮性卵巢癌組織和腹膜中均高錶達。結論趨化因子 SDF-1及其受體 CXCR4在卵巢癌組織中高錶達,通過自分泌作用,可能刺激卵巢癌細胞的過度生長;SDF-1在腹膜組織高錶達,通過徬分泌作用,可能介導錶達 CXCR4的卵巢癌細胞嚮腹腔內轉移。
목적:탐토복강미배경여란소상피성암복강전이관계적연구。방법채용 RT-PCR 법급면역조화법검측란소상피성암조직상응추화인자수체급기배체적표체정황,복막조직상응배체적표체정황,이게시추화인자개도상피성란소암복강내전이궤제。결과추화인자수체 CXCR4재란소상피성암조직중표체명현고우기타추화인자수체표체(P <0.01);추화인자수체 CX-CR4적배체 SDF-1재상피성란소암조직화복막중균고표체。결론추화인자 SDF-1급기수체 CXCR4재란소암조직중고표체,통과자분비작용,가능자격란소암세포적과도생장;SDF-1재복막조직고표체,통과방분비작용,가능개도표체 CXCR4적란소암세포향복강내전이。
Objective To discuss the relationship between the abdominal microenvironment with abdominal cavity metastasis of epithelial ovarian cancer.Methods In order to reveal the mechanism of chemokines mediating epithelial ovarian cancer abdominal cavity metastasis,the expressions of chemokine receptor and its ligand in the epithelial ovarian carcinoma tissue and the peritoneal tissue were detected by RT-PCR and immunohistochemical.Results The expression of chemokine receptor CXCR4 in the epithelial ovarian carcinoma tissue was significantly higher than that of other chemokine receptors (P <0.01).The CXCR4 ligand SDF-1 was high-expressed in the epithelial ovarian carcinoma tissue and the peritoneal tissue.Conclusion The CXCR4 and SDF-1 are high-ex-pressed in the ovarian cancer tissue and may stimulate the excessive growth of ovarian cancer cells by the autocrine function;SDF-1 in the peritoneal tissue is high-expressed and may mediate the ovarian cancer cells expressing CXCR4 transferred to the abdominal cavity.