Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities.
ASCL1
EMT
NEUROD1
POU2F3
SCLC
intratumoral heterogeneity
neuroendocrine
Journal
Cancer cell
ISSN: 1878-3686
Titre abrégé: Cancer Cell
Pays: United States
ID NLM: 101130617
Informations de publication
Date de publication:
08 03 2021
08 03 2021
Historique:
received:
15
06
2020
revised:
28
10
2020
accepted:
14
12
2020
pubmed:
23
1
2021
medline:
29
9
2021
entrez:
22
1
2021
Statut:
ppublish
Résumé
Despite molecular and clinical heterogeneity, small cell lung cancer (SCLC) is treated as a single entity with predictably poor results. Using tumor expression data and non-negative matrix factorization, we identify four SCLC subtypes defined largely by differential expression of transcription factors ASCL1, NEUROD1, and POU2F3 or low expression of all three transcription factor signatures accompanied by an Inflamed gene signature (SCLC-A, N, P, and I, respectively). SCLC-I experiences the greatest benefit from the addition of immunotherapy to chemotherapy, while the other subtypes each have distinct vulnerabilities, including to inhibitors of PARP, Aurora kinases, or BCL-2. Cisplatin treatment of SCLC-A patient-derived xenografts induces intratumoral shifts toward SCLC-I, supporting subtype switching as a mechanism of acquired platinum resistance. We propose that matching baseline tumor subtype to therapy, as well as manipulating subtype switching on therapy, may enhance depth and duration of response for SCLC patients.
Identifiants
pubmed: 33482121
pii: S1535-6108(20)30662-0
doi: 10.1016/j.ccell.2020.12.014
pmc: PMC8143037
mid: NIHMS1661620
pii:
doi:
Substances chimiques
Transcription Factors
0
Cisplatin
Q20Q21Q62J
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
346-360.e7Subventions
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA213274
Pays : United States
Organisme : NCI NIH HHS
ID : R50 CA243698
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA207295
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA070907
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009666
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA215845
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA213273
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA034196
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA213338
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests C.M.G. reports research funding from AstraZeneca. S.H. reports consulting/honoraria from Qiagen, Boehringer Ingelheim and travel funding from Roche. B.Y.Z. and D.S.S. are employees of Genentech, Inc. G.F. is an employee of AstraZeneca and has stock ownership in AstraZeneca. B.G. reports research funding from ISA Pharm, Cue Bio, Pfizer, and Medimmune. I.I.W. reports consulting/advisory roles for Medscape, MSD, Genentech/Roche, PlatformQ Health, Pfizer, Bayer, Bristol-Myers Squibb, AstraZeneca/Medimmune, HTG Molecular, Asuragen, Merck, GlaxoSmithKline, Guardant Health, Oncocyte, and MSD, research support from Genentech, Oncoplex, HTG Molecular, DepArray, Merck, Bristol-Myers Squibb, Medimmune, Adapative, Adaptimmune, EMD Serono, Pfizer, Takeda, Amgen, Karus, Johnson & Johnson, Bayer, Iovance, 4D, Novartis and Akoya. J.V.H. serves on advisory committees for AstraZeneca, Bristol-Myers Squibb, GlaxoSmithKline, Guardant Health, Kairos Venture Investments, BrightPath Biotherapeutics, Hengrui Therapeutics, Eli Lilly, Spectrum, EMD Serono, Roche, and Foundation One Medicine and has research support from AstraZeneca, Spectrum, and Checkmate Pharmaceuticals, as well as royalties/licensing fees from Spectrum and Bio-Tree Systems. L.A.B. serves on advisory committees for AstraZeneca, AbbVie, GenMab, BergenBio, Pharma Mar SA, Sierra Oncology, Merck, Bristol-Myers Squibb, Genentech, and Pfizer and has research support from AbbVie, AstraZeneca, GenMab, Sierra Oncology, Tolero Pharmaceuticals. C.M.G., L.A.B., and J.V.H. have pending patent applications for SCLC subtyping U.S. 62/895,322. Otherwise, there are no pertinent financial or non-financial conflicts of interest to report.
Références
Nat Biotechnol. 2019 Jul;37(7):773-782
pubmed: 31061481
Clin Cancer Res. 2018 Jan 15;24(2):360-369
pubmed: 29118061
Lancet Oncol. 2017 Oct;18(10):e563
pubmed: 28844817
Nat Rev Cancer. 2019 May;19(5):289-297
pubmed: 30926931
J Thorac Oncol. 2020 Apr;15(4):618-627
pubmed: 31870883
Cancer Discov. 2019 Oct;9(10):1372-1387
pubmed: 31416802
Oncotarget. 2017 Apr 25;8(17):28575-28587
pubmed: 28212573
Nature. 2015 Aug 6;524(7563):47-53
pubmed: 26168399
N Engl J Med. 2018 Dec 6;379(23):2220-2229
pubmed: 30280641
Oncotarget. 2017 Sep 1;8(43):73419-73432
pubmed: 29088717
Lancet Oncol. 2016 Jul;17(7):883-895
pubmed: 27269741
Cancer Discov. 2012 Sep;2(9):798-811
pubmed: 22961666
Nature. 2018 Aug;560(7719):494-498
pubmed: 30089906
J Clin Invest. 2017 Aug 1;127(8):2930-2940
pubmed: 28650338
Nat Med. 2018 Aug;24(8):1143-1150
pubmed: 30038220
J Clin Oncol. 2019 Feb 1;37(4):318-327
pubmed: 30557521
Clin Cancer Res. 2019 Jan 1;25(1):346-357
pubmed: 30257981
Cell Rep. 2016 Aug 2;16(5):1259-1272
pubmed: 27452466
Cancer Cell. 2017 Feb 13;31(2):270-285
pubmed: 28089889
Am Soc Clin Oncol Educ Book. 2018 May 23;38:682-695
pubmed: 30231367
J Clin Oncol. 2017 Oct 10;35(29):3338-3346
pubmed: 28817371
Clin Cancer Res. 2012 Jun 1;18(11):3163-9
pubmed: 22496272
J Clin Oncol. 2018 Aug 10;36(23):2386-2394
pubmed: 29906251
PLoS One. 2014 Jun 24;9(6):e100249
pubmed: 24959847
J Thorac Oncol. 2020 May;15(5):777-791
pubmed: 32068166
Clin Cancer Res. 2017 Jan 15;23(2):523-535
pubmed: 27440269
Oncotarget. 2016 Nov 22;7(47):76534-76550
pubmed: 27708213
Cell. 2015 Jan 15;160(1-2):48-61
pubmed: 25594174
Clin Cancer Res. 2016 Feb 1;22(3):609-20
pubmed: 26420858
Nat Methods. 2015 May;12(5):453-7
pubmed: 25822800
Mol Cancer Ther. 2018 Jan;17(1):196-203
pubmed: 29079710
J Thorac Oncol. 2020 Feb;15(2):274-287
pubmed: 31655296
Transl Lung Cancer Res. 2018 Feb;7(1):32-49
pubmed: 29535911
Cancer Res. 1985 Jun;45(6):2924-30
pubmed: 2985258
J Natl Cancer Inst. 2016 Oct 5;109(1):
pubmed: 27707838
Cell Rep. 2019 Jun 11;27(11):3345-3358.e4
pubmed: 31189116
Lung Cancer. 2011 Dec;74(3):481-5
pubmed: 21620511
Nat Cancer. 2020 Apr;1:423-436
pubmed: 33521652
Cancer. 2015 Mar 1;121(5):664-72
pubmed: 25336398
Genes Dev. 2018 Jul 1;32(13-14):915-928
pubmed: 29945888
Cancer Discov. 2019 May;9(5):646-661
pubmed: 30777870
Nat Med. 2014 Aug;20(8):897-903
pubmed: 24880617
J Thorac Oncol. 2020 Dec;15(12):1823-1835
pubmed: 33011388
Nat Biotechnol. 2018 Jun;36(5):411-420
pubmed: 29608179
Mol Cancer Ther. 2019 Nov;18(11):1926-1936
pubmed: 31649014
Nature. 2017 May 18;545(7654):360-364
pubmed: 28489825
Lancet. 2019 Nov 23;394(10212):1929-1939
pubmed: 31590988
Expert Opin Biol Ther. 2019 May;19(5):423-432
pubmed: 30855195
Cancer Cell. 2020 Jul 13;38(1):60-78.e12
pubmed: 32473656
Cancer Discov. 2015 Aug;5(8):860-77
pubmed: 26069186
Clin Cancer Res. 2019 Aug 15;25(16):5107-5121
pubmed: 31164374
Clin Cancer Res. 2013 Jan 1;19(1):279-90
pubmed: 23091115
J Natl Cancer Inst. 2016 May 31;108(10):
pubmed: 27247353
Cancer Discov. 2019 Jun;9(6):722-737
pubmed: 31015319
Genome Biol. 2019 Mar 19;20(1):59
pubmed: 30890159
Sci Rep. 2013;3:1911
pubmed: 23714854
Cancer Immunol Immunother. 2017 Nov;66(11):1425-1436
pubmed: 28660319
Cancer Res. 1985 Jun;45(6):2913-23
pubmed: 2985257
Cancer Cell. 2018 May 14;33(5):853-861.e4
pubmed: 29731394
J Med Chem. 2019 Mar 14;62(5):2708-2719
pubmed: 30735385
Cancer Discov. 2019 Jan;9(1):34-45
pubmed: 30297358