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. 2019 Oct 4;7(3):219–232. doi: 10.1016/j.ajur.2019.09.005

Table 2.

Somatic mutations in AR-associated NCoA and NCoR coregulators in clinical PCa. COSMIC and cBio databases were queried for somatic mutations in genes that encode AR-associated NCoAs and NCoRs (28). The COSMIC database was queried via the Cancer browser, selecting for “prostate cancer” and “carcinoma” histology, and retrieving only data from genome-wide sequencing efforts. For cBIO analysis, datasets analyses are marked by first author of study that was examined.

Genes COSMIC
cBIO
# ADT-naïve ADT-naïve ADT-naïve ADT-naïve ADT-naïve + CRPC CRPC CRPC ADT-naïve CRPC
n=1 976 Barbieri n=112 Fraser n=477 TCGA n=333 Armenia n=1 013 Abida n=444 Beltran n=114 n=922 n=558
% # % # % # % # % # % # % average% average%
NCOA1 10 0.51 0 0.00 0 0.00 2 0.60 6 0.59 2 0.45 0 0.00 0.20 0.23
NCOA2 9 0.46 2 1.79 1 0.21 1 0.30 8 0.79 4 0.90 0 0.00 0.77 0.45
NCOA3 11 0.56 1 0.89 3 0.63 2 0.60 6 0.59 2 0.45 1 0.88 0.71 0.66
NCOA4 0 0.00 0 0.00 0 0.00 2 0.60 3 0.30 1 0.23 0 0.00 0.20 0.11
NCOA6 17 0.86 1 0.89 1 0.21 2 0.60 10 0.99 4 0.90 0 0.00 0.57 0.45
NCOR1 19 0.96 2 1.79 4 0.84 6 1.80 26 2.57 13 2.93 2 1.75 1.48 2.34
NCOR2 28 1.42 1 0.89 1 0.21 0 0.00 23 2.27 14 3.15 1 0.88 0.37 2.02

Corresponding cBIO annotations is as follows: Barbieri, Prostate Adenocarcinoma (Broad/Cornell, Nature Genetics 2012); Fraser, Prostate Adenocarcinoma (CPC-Gene, Nature 2017); Armenia, Prostate Adenocarcinoma (MSKCC/DFCI, Nature Genetics 2018); Abida, Metastatic Prostate Adenocarcimoma, SU2C/PCF Dream Team, PNAS 2019; Beltran, Neuroendocrine Prostate Cancer (Multi-institute, Nature Medicine 2016). Note that the study of Armenia et al. includes data from 680 ADT-naïve and 333 CRPC cases; data from this study have not been taken into consideration in determining average %.

#, number of somatic mutations/study that affects the gene for which the symbol is listed.

%, percentage of cases/study that harbor somatic mutation that affects the gene for which the symbol is listed.

Average %, average of percentage of mutations from studies on either ADT-naïve PCa or CRPC specimens; ADT, androgen deprivation therapy; CRPC, castration-resistant PCa; PCa, prostate cancer.