4.4 Article

CD40 Signal Regulates CXCR4 Mediating Ovarian Carcinoma Cell Migration: Implications for Extrapelvic Metastastic Factors

Journal

ONCOLOGY RESEARCH
Volume 20, Issue 9, Pages 383-392

Publisher

COGNIZANT COMMUNICATION CORP
DOI: 10.3727/096504013X13657689382653

Keywords

Ovarian cancer; CD40; CXCR4; Migration; Pelvic metastasis

Categories

Funding

  1. National Natural Science Foundation of China [81101556]
  2. Research Innovation Project for University Graduate Student in Jiangsu Province [CXZZ11_0110]
  3. Suzhou social development project [SYSD2011084]
  4. Jiangsu Province's Key Laboratory of Medicine [XK201135]

Ask authors/readers for more resources

Ovarian carcinomas are highly invasive, especially in the peritoneal cavity. SDF-1 alpha and its receptor, CXCR4, play a crucial role in migration of cancer cells. Here, SDF-1 alpha directed HO8910 cell migration, but not SKOV3 cells. After being educated to express CXCR4 in vivo or by treating with sCD40L, SDF-1 alpha reexhibited the ability of directing SKOV3 cell migration, which could be antagonized by CXCR4-neutralizing antibody. Furthermore, concomitant expression of CXCR4/CD40 in ovarian carcinoma tissues had stronger correlation with pelvic metastasis than did each alone. It is suggest that SDF-1 alpha acts through CXCR4 to induce ovarian cancer cell migration, which could be facilitated by CD40 activation. Simultaneously examining the expression of CXCR4 and CD40 will provide valuable diagnosis of pelvic metastasis for ovarian carcinomas.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available