z-logo
open-access-imgOpen Access
Do drugs that target mTOR generate CCN2‐mediated fibrogenic side effects?
Author(s) -
Leask Andrew
Publication year - 2019
Publication title -
journal of cell communication and signaling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 44
eISSN - 1873-961X
pISSN - 1873-9601
DOI - 10.1007/s12079-019-00520-y
Subject(s) - pi3k/akt/mtor pathway , discovery and development of mtor inhibitors , medicine , sirolimus , fibrosis , cancer research , lung , pharmacology , bioinformatics , signal transduction , biology , microbiology and biotechnology
mTOR, the target of rapamycin, has been promoted as a potential target for cancers, transplantations and even lung fibrosis. However, paradoxically, targeting mTOR has been reported to result in profibrotic side effects. Some recent publications highlight why this might be.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here