TY - JOUR
T1 - Identification of gene expression levels in primary melanoma associated with clinically meaningful characteristics
AU - Gorlov, Ivan
AU - Orlow, Irene
AU - Ringelberg, Carol
AU - Hernando, Eva
AU - Ernstoff, Marc S.
AU - Cheng, Chao
AU - Her, Stephanie
AU - Parker, Joel S.
AU - Thompson, Cheryl L.
AU - Gerstenblith, Meg R.
AU - Berwick, Marianne
AU - Amos, Christopher
N1 - Funding Information:
This work was supported in part by the National Institutes of Health P01 CA206980-01A1 grant and P30 CA008748 grant to Memorial Sloan Kettering Cancer Center. The authors also received funding from the Prouty pilot program of the Norris Cotton Cancer Center P30CA0123108, the Char and Chuck Fowler Family Foundation, and the New Mexico Medical Trust.
Publisher Copyright:
© 2018 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Factors influencing melanoma survival include sex, age, clinical stage, lymph node involvement, as well as Breslow thickness, presence of tumor-infiltrating lymphocytes based on histological analysis of primary melanoma, mitotic rate, and ulceration. Identification of genes whose expression in primary tumors is associated with these key tumor/patient characteristics can shed light on molecular mechanisms of melanoma survival. Here, we show results from a gene expression analysis of formalin-fixed paraffin-embedded primary melanomas with extensive clinical annotation. The Cancer Genome Atlas data on primary melanomas were used for validation of nominally significant associations. We identified five genes that were significantly associated with the presence of tumor-infiltrating lymphocytes in the joint analysis after adjustment for multiple testing: IL1R2, PPL, PLA2G3, RASAL1, and SGK2. We also identified two genes significantly associated with melanoma metastasis to the regional lymph nodes (PIK3CG and IL2RA), and two genes significantly associated with sex (KDM5C and KDM6A). We found that LEF1 was significantly associated with Breslow thickness and CCNA2 and UBE2T with mitosis. RAD50 was the gene most significantly associated with survival, with a higher level of expression associated with worse survival.
AB - Factors influencing melanoma survival include sex, age, clinical stage, lymph node involvement, as well as Breslow thickness, presence of tumor-infiltrating lymphocytes based on histological analysis of primary melanoma, mitotic rate, and ulceration. Identification of genes whose expression in primary tumors is associated with these key tumor/patient characteristics can shed light on molecular mechanisms of melanoma survival. Here, we show results from a gene expression analysis of formalin-fixed paraffin-embedded primary melanomas with extensive clinical annotation. The Cancer Genome Atlas data on primary melanomas were used for validation of nominally significant associations. We identified five genes that were significantly associated with the presence of tumor-infiltrating lymphocytes in the joint analysis after adjustment for multiple testing: IL1R2, PPL, PLA2G3, RASAL1, and SGK2. We also identified two genes significantly associated with melanoma metastasis to the regional lymph nodes (PIK3CG and IL2RA), and two genes significantly associated with sex (KDM5C and KDM6A). We found that LEF1 was significantly associated with Breslow thickness and CCNA2 and UBE2T with mitosis. RAD50 was the gene most significantly associated with survival, with a higher level of expression associated with worse survival.
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U2 - 10.1097/CMR.0000000000000473
DO - 10.1097/CMR.0000000000000473
M3 - Article
C2 - 29975213
AN - SCOPUS:85053937935
SN - 0960-8931
VL - 28
SP - 380
EP - 389
JO - Melanoma Research
JF - Melanoma Research
IS - 5
ER -