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Multiomics Profiling Distinguishes Sebaceous Carcinoma from Benign Sebaceous Neoplasms and Provides Insight into the Genetic Evolution of Sebaceous Carcinogenesis.

Publication ,  Journal Article
Starrett, GJ; Baikie, BC; Stoff, BK; Grossniklaus, HE; Van Buren, I; Berry, EG; Novoa, RA; Rieger, KE; Sarin, KY; Lynch, CF; Royer, MC; Yu, KJ ...
Published in: Clin Cancer Res
November 1, 2024

PURPOSE: Sebaceous carcinoma is the third most common nonkeratinocyte skin cancer in the United States with 1,000 cases per year. The clinicopathologic features of sebaceous carcinoma and benign sebaceous neoplasms (adenomas, sebaceomas) can overlap, highlighting the need for molecular biomarkers to improve classification. This study describes the genomic and transcriptomic landscape of sebaceous neoplasms in order to understand tumor etiology and biomarkers relevant for diagnosis and treatment. EXPERIMENTAL DESIGN: We performed whole-genome sequencing (WGS) and whole-transcriptome sequencing (WTS) of sebaceous neoplasms from six academic and two federal healthcare facilities in the United States diagnosed between January 1, 1999, and December 31, 2021. RESULTS: We evaluated 98 sebaceous neoplasms: 64 tumors (32 adenomas, 2 sebaceomas, 5 atypical sebaceous neoplasms, 25 carcinomas) had sufficient material for WGS, 96 tumors (42 adenomas, 11 sebaceomas, 8 atypical sebaceous neoplasms, 35 carcinomas) had sufficient material for WTS, and 62 tumors (31 adenomas, 2 sebaceomas, 5 atypical sebaceous neoplasms, 24 carcinomas) had sufficient material for combined WGS and WTS. Overall, we found decreased cholesterol biosynthesis and increased TP53 mutations, copy number gains (chromosome 6, 8q, and/or 18), and tumor mutation burden-high (>10 mutations/MB) in carcinomas compared to adenomas. Although diminished compared to adenomas, most carcinomas still had higher cholesterol biosynthesis than nonmalignant skin. Multiomics profiling also supported a precancerous model of tumor evolution with sebaceomas and atypical sebaceous neoplasms being likely intermediate lesions. CONCLUSIONS: The study findings highlight key diagnostic biomarkers for sebaceous carcinoma and suggest that immunotherapy and modulation of cholesterol biosynthesis could be effective treatment strategies.

Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

November 1, 2024

Volume

30

Issue

21

Start / End Page

4887 / 4899

Location

United States

Related Subject Headings

  • Whole Genome Sequencing
  • Transcriptome
  • Sebaceous Gland Neoplasms
  • Oncology & Carcinogenesis
  • Mutation
  • Multiomics
  • Middle Aged
  • Male
  • Humans
  • Gene Expression Profiling
 

Citation

APA
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MLA
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Starrett, G. J., Baikie, B. C., Stoff, B. K., Grossniklaus, H. E., Van Buren, I., Berry, E. G., … Sargen, M. R. (2024). Multiomics Profiling Distinguishes Sebaceous Carcinoma from Benign Sebaceous Neoplasms and Provides Insight into the Genetic Evolution of Sebaceous Carcinogenesis. Clin Cancer Res, 30(21), 4887–4899. https://doi.org/10.1158/1078-0432.CCR-24-1327
Starrett, Gabriel J., Brittany C. Baikie, Benjamin K. Stoff, Hans E. Grossniklaus, Inga Van Buren, Elizabeth G. Berry, Roberto A. Novoa, et al. “Multiomics Profiling Distinguishes Sebaceous Carcinoma from Benign Sebaceous Neoplasms and Provides Insight into the Genetic Evolution of Sebaceous Carcinogenesis.Clin Cancer Res 30, no. 21 (November 1, 2024): 4887–99. https://doi.org/10.1158/1078-0432.CCR-24-1327.
Starrett GJ, Baikie BC, Stoff BK, Grossniklaus HE, Van Buren I, Berry EG, et al. Multiomics Profiling Distinguishes Sebaceous Carcinoma from Benign Sebaceous Neoplasms and Provides Insight into the Genetic Evolution of Sebaceous Carcinogenesis. Clin Cancer Res. 2024 Nov 1;30(21):4887–99.
Starrett, Gabriel J., et al. “Multiomics Profiling Distinguishes Sebaceous Carcinoma from Benign Sebaceous Neoplasms and Provides Insight into the Genetic Evolution of Sebaceous Carcinogenesis.Clin Cancer Res, vol. 30, no. 21, Nov. 2024, pp. 4887–99. Pubmed, doi:10.1158/1078-0432.CCR-24-1327.
Starrett GJ, Baikie BC, Stoff BK, Grossniklaus HE, Van Buren I, Berry EG, Novoa RA, Rieger KE, Sarin KY, Lynch CF, Royer MC, Piaskowski ML, Brownell I, Chu EY, Godse R, Chen SC, Yu KJ, Goldstein AM, Engels EA, Sargen MR. Multiomics Profiling Distinguishes Sebaceous Carcinoma from Benign Sebaceous Neoplasms and Provides Insight into the Genetic Evolution of Sebaceous Carcinogenesis. Clin Cancer Res. 2024 Nov 1;30(21):4887–4899.

Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

November 1, 2024

Volume

30

Issue

21

Start / End Page

4887 / 4899

Location

United States

Related Subject Headings

  • Whole Genome Sequencing
  • Transcriptome
  • Sebaceous Gland Neoplasms
  • Oncology & Carcinogenesis
  • Mutation
  • Multiomics
  • Middle Aged
  • Male
  • Humans
  • Gene Expression Profiling