Cortactin recruits FMNL2 to promote actin polymerization and endosome motility in invadopodia formation. (10th April 2018)
- Record Type:
- Journal Article
- Title:
- Cortactin recruits FMNL2 to promote actin polymerization and endosome motility in invadopodia formation. (10th April 2018)
- Main Title:
- Cortactin recruits FMNL2 to promote actin polymerization and endosome motility in invadopodia formation
- Authors:
- Ren, X.L.
Qiao, Y.D.
Li, J.Y.
Li, X.M.
Zhang, D.
Zhang, X.J.
Zhu, X.H.
Zhou, W.J.
Shi, J.
Wang, W.
Liao, W.T.
Ding, Y.Q.
Liang, L. - Abstract:
- Abstract: Recently, invadopodia have been increasingly recognized as important drivers of local invasion and metastasis. Cortactin, as an actin-binding protein, is closely associated with invadopodia through interacting with proteins. Formin-like 2 (FMNL2), a member of diaphanous-related formins which act as nucleation factors, plays an important role in tumor progression. But whether cortactin can interact with FMNL2 to promote invadopodia formation and the role of FMNL2 in invadopodia formation are still unknown. Here we found that cortactin directly bound to FMNL2 and elevated the activities of actin polymerization and recycling endosome motility. FMNL2 was necessary for invadopodia formation and function in CRC cells. The interaction of cortactin and FMNL2 could further promote the invadopodia formation and matrix degradation. The stimulation of EGF/cdc42 enhanced the combination of cortactin and FMNL2 to intensify the numbers of invadopodia and the degrees of matrix degradation. In vivo, induction of invadopodia formation via cortactin is essential for the ability of FMNL2 to promote CRC metastasis. Furthermore, up-regulations of FMNL2 and cortactin were highly linked in CRC tissues. Collectively, our work demonstrates a brand-new mechanism of cortacin and FMNL2 at invadopodia in CRC. Highlights: Cortactin interacts with FMNL2 promotes actin polymerization and endosome activity. FMNL2 is necessary for the formation and function of invadopodia. EGF/Cdc42 enhances theAbstract: Recently, invadopodia have been increasingly recognized as important drivers of local invasion and metastasis. Cortactin, as an actin-binding protein, is closely associated with invadopodia through interacting with proteins. Formin-like 2 (FMNL2), a member of diaphanous-related formins which act as nucleation factors, plays an important role in tumor progression. But whether cortactin can interact with FMNL2 to promote invadopodia formation and the role of FMNL2 in invadopodia formation are still unknown. Here we found that cortactin directly bound to FMNL2 and elevated the activities of actin polymerization and recycling endosome motility. FMNL2 was necessary for invadopodia formation and function in CRC cells. The interaction of cortactin and FMNL2 could further promote the invadopodia formation and matrix degradation. The stimulation of EGF/cdc42 enhanced the combination of cortactin and FMNL2 to intensify the numbers of invadopodia and the degrees of matrix degradation. In vivo, induction of invadopodia formation via cortactin is essential for the ability of FMNL2 to promote CRC metastasis. Furthermore, up-regulations of FMNL2 and cortactin were highly linked in CRC tissues. Collectively, our work demonstrates a brand-new mechanism of cortacin and FMNL2 at invadopodia in CRC. Highlights: Cortactin interacts with FMNL2 promotes actin polymerization and endosome activity. FMNL2 is necessary for the formation and function of invadopodia. EGF/Cdc42 enhances the combination of cortactin and FMNL2 in invadopodia. … (more)
- Is Part Of:
- Cancer letters. Volume 419(2018)
- Journal:
- Cancer letters
- Issue:
- Volume 419(2018)
- Issue Display:
- Volume 419, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 419
- Issue:
- 2018
- Issue Sort Value:
- 2018-0419-2018-0000
- Page Start:
- 245
- Page End:
- 256
- Publication Date:
- 2018-04-10
- Subjects:
- Cortactin -- FMNL2 -- EGF/cdc 42 -- Invadopodia -- Colorectal cancer
Cancer -- Periodicals
Neoplasms -- Periodicals
Cancer -- Périodiques
Electronic journals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03043835/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.canlet.2018.01.023 ↗
- Languages:
- English
- ISSNs:
- 0304-3835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.485000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11587.xml