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Cervicovaginal Metabolome and Tumor Characteristics for Endometrial Cancer Detection and Risk Stratification.
Lorentzen, Georgia M; Laniewski, Pawel; Cui, Haiyan; Mahnert, Nichole D; Mourad, Jamal; Borst, Matthew P; Willmott, Lyndsay; Chase, Dana M; Roe, Denise J; Herbst-Kralovetz, Melissa M.
Afiliação
  • Lorentzen GM; Department of Obstetrics and Gynecology, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona.
  • Laniewski P; Department of Biology & Biochemistry, University of Bath, Bath, United Kingdom.
  • Cui H; Department of Basic Medical Sciences, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona.
  • Mahnert ND; UA Cancer Center, University of Arizona, Tucson, Arizona.
  • Mourad J; Department of Obstetrics and Gynecology, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona.
  • Borst MP; Banner-University Medical Center, Phoenix, Arizona.
  • Willmott L; Department of Obstetrics and Gynecology, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona.
  • Chase DM; Banner-University Medical Center, Phoenix, Arizona.
  • Roe DJ; Department of Obstetrics and Gynecology, College of Medicine-Phoenix, University of Arizona, Phoenix, Arizona.
  • Herbst-Kralovetz MM; Banner-University Medical Center, Phoenix, Arizona.
Clin Cancer Res ; 30(14): 3073-3087, 2024 Jul 15.
Article em En | MEDLINE | ID: mdl-38687603
ABSTRACT

PURPOSE:

Endometrial cancer is highly prevalent and lacking noninvasive diagnostic techniques. Diagnosis depends on histological investigation of biopsy samples. Serum biomarkers for endometrial cancer have lacked sensitivity and specificity. The objective of this study was to investigate the cervicovaginal environment to improve the understanding of metabolic reprogramming related to endometrial cancer and identify potential biomarker candidates for noninvasive diagnostic and prognostic tests. EXPERIMENTAL

DESIGN:

Cervicovaginal lavages were collected from 192 participants with endometrial cancer (n = 66) and non-malignant conditions (n = 108), and global untargeted metabolomics was performed. Using the metabolite data (n = 920), we completed a multivariate biomarker discovery analysis.

RESULTS:

We analyzed grade 1/2 endometrioid carcinoma (n = 53) and other endometrial cancer subtypes (n = 13) to identify shared and unique metabolic signatures between the subtypes. When compared to non-malignant conditions, downregulation of proline (P < 0.0001), tryptophan (P < 0.0001), and glutamate (P < 0.0001) was found among both endometrial cancer groups, relating to key hallmarks of cancer including immune suppression and redox balance. Upregulation (q < 0.05) of sphingolipids, fatty acids, and glycerophospholipids was observed in endometrial cancer in a type-specific manner. Furthermore, cervicovaginal metabolites related to tumor characteristics, including tumor size and myometrial invasion.

CONCLUSIONS:

Our findings provide insights into understanding the endometrial cancer metabolic landscape and improvement in diagnosis. The metabolic dysregulation described in this article linked specific metabolites and pathophysiological mechanisms including cellular proliferation, energy supply, and invasion of neighboring tissues. Furthermore, cervicovaginal metabolite levels related to tumor characteristics, which are used for risk stratification. Overall, development of noninvasive diagnostics can improve both the acceptability and accessibility of diagnosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vagina / Biomarcadores Tumorais / Neoplasias do Endométrio / Metaboloma Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vagina / Biomarcadores Tumorais / Neoplasias do Endométrio / Metaboloma Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article