» Articles » PMID: 20235885

MTOR Signaling in Lymphangioleiomyomatosis

Overview
Date 2010 Mar 19
PMID 20235885
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The protein mammalian target of rapamycin (mTOR) plays a central role in cell growth and proliferation. Excessive mTOR activity is a prominent feature of many neoplasms and hamartoma syndromes, including lymphangioleiomyomatosis (LAM), a destructive lung disease that causes progressive respiratory failure in women. Although pharmacological inhibitors of mTOR should directly target the pathogenesis of these disorders, their clinical efficacy has been suboptimal. Recent scientific findings reviewed here have greatly improved our understanding of mTOR signaling mechanisms, provided new insights into the control of cell growth and proliferation, and facilitated the development of new therapeutic approaches in LAM, as well as other neoplastic disorders that exhibit excessive mTOR activity.

Citing Articles

Lymphangioleiomyomatosis and pregnancy: a mini-review.

Zhou J, Diao M Arch Gynecol Obstet. 2024; 309(6):2339-2346.

PMID: 38594407 PMC: 11147845. DOI: 10.1007/s00404-024-07478-2.


Prdx5 in the Regulation of Tuberous Sclerosis Complex Mutation-Induced Signaling Mechanisms.

Bovari-Biri J, Abdelwahab E, Garai K, Pongracz J Cells. 2023; 12(13).

PMID: 37443747 PMC: 10340296. DOI: 10.3390/cells12131713.


Cystic Lung Disease Presenting as Recurrent Non-traumatic Chylothorax: Case Report and a Mini-Review.

Gupta S, Paul V Cureus. 2023; 15(6):e40217.

PMID: 37435256 PMC: 10332385. DOI: 10.7759/cureus.40217.


Tuberous sclerosis complex associated lymphangioleiomyomatosis.

Han Z, Xue X, Wang J, Lu D QJM. 2023; 116(10):873-874.

PMID: 37286375 PMC: 10593382. DOI: 10.1093/qjmed/hcad125.


Raising the Flag for Mast Cells as a Novel Target in Lymphangioleiomyomatosis.

Goldklang M Am J Respir Crit Care Med. 2021; 204(4):387-389.

PMID: 33951405 PMC: 8480237. DOI: 10.1164/rccm.202104-0872ED.


References
1.
Murata K, Wu J, Brautigan D . B cell receptor-associated protein alpha4 displays rapamycin-sensitive binding directly to the catalytic subunit of protein phosphatase 2A. Proc Natl Acad Sci U S A. 1997; 94(20):10624-9. PMC: 23426. DOI: 10.1073/pnas.94.20.10624. View

2.
Inui S, Sanjo H, Maeda K, Yamamoto H, Miyamoto E, Sakaguchi N . Ig receptor binding protein 1 (alpha4) is associated with a rapamycin-sensitive signal transduction in lymphocytes through direct binding to the catalytic subunit of protein phosphatase 2A. Blood. 1998; 92(2):539-46. View

3.
NANAHOSHI M, Nishiuma T, Tsujishita Y, Hara K, Inui S, Sakaguchi N . Regulation of protein phosphatase 2A catalytic activity by alpha4 protein and its yeast homolog Tap42. Biochem Biophys Res Commun. 1998; 251(2):520-6. DOI: 10.1006/bbrc.1998.9493. View

4.
Peterson R, Desai B, Hardwick J, Schreiber S . Protein phosphatase 2A interacts with the 70-kDa S6 kinase and is activated by inhibition of FKBP12-rapamycinassociated protein. Proc Natl Acad Sci U S A. 1999; 96(8):4438-42. PMC: 16350. DOI: 10.1073/pnas.96.8.4438. View

5.
Brugarolas J, Lei K, Hurley R, Manning B, Reiling J, Hafen E . Regulation of mTOR function in response to hypoxia by REDD1 and the TSC1/TSC2 tumor suppressor complex. Genes Dev. 2004; 18(23):2893-904. PMC: 534650. DOI: 10.1101/gad.1256804. View