BCL-X


Journal

Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937

Informations de publication

Date de publication:
09 03 2022
Historique:
received: 05 01 2022
accepted: 19 02 2022
entrez: 9 3 2022
pubmed: 10 3 2022
medline: 13 4 2022
Statut: epublish

Résumé

KRAS mutations are the most common oncogenic drivers. Sotorasib (AMG510), a covalent inhibitor of KRAS

Identifiants

pubmed: 35260176
doi: 10.1186/s13045-022-01241-3
pii: 10.1186/s13045-022-01241-3
pmc: PMC8905794
doi:

Substances chimiques

bcl-X Protein 0
DT2216 0
KRAS protein, human 0
Piperazines 0
Proto-Oncogene Proteins p21(ras) EC 3.6.5.2
Pyridines 0
Pyrimidines 0
sotorasib 2B2VM6UC8G

Types de publication

Letter Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

Subventions

Organisme : NCI NIH HHS
ID : R01 CA242003
Pays : United States

Informations de copyright

© 2022. The Author(s).

Références

Moore AR, Rosenberg SC, McCormick F, Malek S. RAS-targeted therapies: Is the undruggable drugged? Nat Rev Drug Discov. 2020;19(8):533–52.
doi: 10.1038/s41573-020-0068-6
Canon J, Rex K, Saiki AY, Mohr C, Cooke K, Bagal D, et al. The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity. Nature. 2019;575(7781):217–23.
doi: 10.1038/s41586-019-1694-1
Ryan MB, Fece de la Cruz F, Phat S, Myers DT, Wong E, Shahzade HA, et al. Vertical pathway inhibition overcomes adaptive feedback resistance to KRAS. Clin Cancer Res. 2020;26(7):1633–43.
Misale S, Fatherree JP, Cortez E, Li C, Bilton S, Timonina D, et al. KRAS G12C NSCLC models are sensitive to direct targeting of KRAS in combination with PI3K inhibition. Clin Cancer Res. 2019;25(2):796–807.
doi: 10.1158/1078-0432.CCR-18-0368
Mason KD, Carpinelli MR, Fletcher JI, Collinge JE, Hilton AA, Ellis S, et al. Programmed anuclear cell death delimits platelet life span. Cell. 2007;128(6):1173–86.
doi: 10.1016/j.cell.2007.01.037
Zhang H, Nimmer PM, Tahir SK, Chen J, Fryer RM, Hahn KR, et al. Bcl-2 family proteins are essential for platelet survival. Cell Death Differ. 2007;14(5):943–51.
doi: 10.1038/sj.cdd.4402081
Schoenwaelder SM, Jarman KE, Gardiner EE, Hua M, Qiao J, White MJ, et al. Bcl-xL-inhibitory BH3 mimetics can induce a transient thrombocytopathy that undermines the hemostatic function of platelets. Blood. 2011;118(6):1663–74.
doi: 10.1182/blood-2011-04-347849
Khan S, Zhang X, Lv D, Zhang Q, He Y, Zhang P, et al. A selective BCL-X L PROTAC degrader achieves safe and potent antitumor activity. Nat Med. 2019;25(12):1938–47.
doi: 10.1038/s41591-019-0668-z
He Y, Koch R, Budamagunta V, Zhang P, Zhang X, Khan S, et al. DT2216-a Bcl-xL-specific degrader is highly active against Bcl-xL-dependent T cell lymphomas. J Hematol Oncol. 2020;13(1):95.
doi: 10.1186/s13045-020-00928-9
Zhang X, Thummuri D, Liu X, Hu W, Zhang P, Khan S, et al. Discovery of PROTAC BCL-X L degraders as potent anticancer agents with low on-target platelet toxicity. Eur J Med Chem. 2020;192:112186.
doi: 10.1016/j.ejmech.2020.112186
Kasper S, Breitenbuecher F, Reis H, Brandau S, Worm K, Köhler J, et al. Oncogenic RAS simultaneously protects against anti-EGFR antibody-dependent cellular cytotoxicity and EGFR signaling blockade. Oncogene. 2013;32(23):2873–81.
doi: 10.1038/onc.2012.302
Luciano F, Jacquel A, Colosetti P, Herrant M, Cagnol S, Pages G, et al. Phosphorylation of Bim-EL by Erk1/2 on serine 69 promotes its degradation via the proteasome pathway and regulates its proapoptotic function. Oncogene. 2003;22(43):6785–93.
doi: 10.1038/sj.onc.1206792

Auteurs

Sajid Khan (S)

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA. khansajid@cop.ufl.edu.

Janet Wiegand (J)

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA.

Peiyi Zhang (P)

Department of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, USA.

Wanyi Hu (W)

Department of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, USA.

Dinesh Thummuri (D)

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA.

Vivekananda Budamagunta (V)

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA.
Department of Neuroscience, College of Medicine, University of Florida, Gainesville, FL, USA.
Genetics and Genomics Graduate Program, Genetics Institute, College of Medicine, University of Florida, Gainesville, FL, USA.

Nan Hua (N)

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA.

Lingtao Jin (L)

Department of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL, USA.

Carmen J Allegra (CJ)

Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.

Scott E Kopetz (SE)

Department of Gastrointestinal Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Maria Zajac-Kaye (M)

Department of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL, USA.

Frederic J Kaye (FJ)

Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.

Guangrong Zheng (G)

Department of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, USA.

Daohong Zhou (D)

Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA. zhoudaohong@cop.ufl.edu.

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Classifications MeSH