PMID- 19629070 OWN - NLM STAT- MEDLINE DCOM- 20090811 LR - 20220413 IS - 1474-1768 (Electronic) IS - 1474-175X (Linking) VI - 9 IP - 8 DP - 2009 Aug TI - Targeting PI3K signalling in cancer: opportunities, challenges and limitations. PG - 550-62 LID - 10.1038/nrc2664 [doi] AB - There are ample genetic and laboratory studies that suggest the PI3K-Akt pathway is vital to the growth and survival of cancer cells. Inhibitors targeting this pathway are entering the clinic at a rapid pace. In this Review, the therapeutic potential of drugs targeting PI3K-Akt signalling for the treatment of cancer is discussed. I focus on the advantages and drawbacks of different treatment strategies for targeting this pathway, the cancers that might respond best to these therapies and the challenges and limitations that confront their clinical development. FAU - Engelman, Jeffrey A AU - Engelman JA AD - Massachusetts General Hospital Cancer Center, Boston, Massachusetts 02129, USA. jengelman@partners.org LA - eng PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Review PL - England TA - Nat Rev Cancer JT - Nature reviews. Cancer JID - 101124168 RN - 0 (Antineoplastic Agents) RN - 0 (Protein Kinase Inhibitors) RN - EC 2.7.- (Protein Kinases) RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.11.1 (Proto-Oncogene Proteins c-akt) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) SB - IM MH - Antineoplastic Agents/pharmacology/*therapeutic use MH - Humans MH - Neoplasms/*drug therapy/*etiology/pathology MH - Phosphatidylinositol 3-Kinases/*physiology MH - Protein Kinase Inhibitors/pharmacology/*therapeutic use MH - Protein Kinases/physiology MH - Proto-Oncogene Proteins c-akt/*physiology MH - Signal Transduction/drug effects/*physiology MH - TOR Serine-Threonine Kinases RF - 159 EDAT- 2009/07/25 09:00 MHDA- 2009/08/12 09:00 CRDT- 2009/07/25 09:00 PHST- 2009/07/25 09:00 [entrez] PHST- 2009/07/25 09:00 [pubmed] PHST- 2009/08/12 09:00 [medline] AID - nrc2664 [pii] AID - 10.1038/nrc2664 [doi] PST - ppublish SO - Nat Rev Cancer. 2009 Aug;9(8):550-62. doi: 10.1038/nrc2664.