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Cited by 337

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Effective and selective targeting of leukemia cells using a TORC1/2 kinase inhibitor

Open access
Janes, Matthew R, Limon, Jose J, So, Lomon, Chen, Jing, Lim, Raymond J, Chavez, Melissa A, Vu, Collin, Lilly, Michael B, Mallya, Sharmila, Ong, S Tiong, Konopleva, Marina, Martin, Michael B, Ren, Pingda, Liu, Yi, Rommel, Christian, Fruman, David A·2010·Nature Medicine

Abstract

Targeting the mammalian target of rapamycin (mTOR) protein is a promising strategy for cancer therapy. The mTOR kinase functions in two complexes, TORC1 (target of rapamycin complex-1) and TORC2 (target of rapamycin complex-2); however, neither of these complexes is fully inhibited by the allosteric inhibitor rapamycin or its analogs. We compared rapamycin with PP242, an inhibitor of the active site of mTOR in both TORC1 and TORC2 (hereafter referred to as TORC1/2), in models of acute leukemia harboring the Philadelphia chromosome (Ph) translocation. We demonstrate that PP242, but not rapamycin, causes death of mouse and human leukemia cells. In vivo, PP242 delays leukemia onset and augments the effects of the current front-line tyrosine kinase inhibitors more effectively than does rapamycin. Unexpectedly, PP242 has much weaker effects than rapamycin on the proliferation and function of normal lymphocytes. PI-103, a less selective TORC1/2 inhibitor that also targets phosphoinositide 3-kinase (PI3K), is more immunosuppressive than PP242. These findings establish that Ph+ transformed cells are more sensitive than normal lymphocytes to selective TORC1/2 inhibitors and support the development of such inhibitors for leukemia therapy.

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Crossref · 10.1038/nm.2091

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Metadata

Authors
Janes, M. R., Limon, J. J., So, L., Chen, J., Lim, R. J., Chavez, M. A., Vu, C., Lilly, M. B., Mallya, S., Ong, S. T., Konopleva, M., Martin, M. B., Ren, P., Liu, Y., Rommel, C., & Fruman, D. A.
Venue
Nature Medicine
Published
2010-01-13
Volume
16
Issue
2
Pages
205-213
ISSN
  • 1078-8956 (ISSN-L)
  • 1546-170X
OpenAlex
W2115655607
Cited by
337
References
6
FWCI
19.85
Type
journal article
Language
en
Open access
green

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