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PTGES3 is a Putative Prognostic Marker in Breast Cancer.
Adekeye, Adeseye; Agarwal, Divyansh; Nayak, Anupma; Tchou, Julia.
Afiliação
  • Adekeye A; Division of Endocrine and Oncologic Surgery, Department of Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania. Electronic address: adeseye.adekeye@jefferson.edu.
  • Agarwal D; Division of Endocrine and Oncologic Surgery, Department of Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania; Medical Scientist Training Program, Genomics and Computational Biology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Nayak A; Dept. of Pathology and Laboratory Medicine, Perelman School of Medicine, Philadelphia, Pennsylvania.
  • Tchou J; Division of Endocrine and Oncologic Surgery, Department of Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania. Electronic address: Julia.Tchou@pennmedicine.upenn.edu.
J Surg Res ; 271: 154-162, 2022 03.
Article em En | MEDLINE | ID: mdl-34920330
ABSTRACT

BACKGROUND:

The COX/prostaglandin (COX/PG) pathway plays a role in cancer pathogenesis via the production of prostaglandin E2 (PGE2). In breast cancer, the expression patterns of the COX/PG pathway enzymes involved in PGE2 synthesis are not well defined. MATERIALS AND

METHODS:

Using the Cancer Genome Atlas data, we analyzed the expression patterns of cyclooxygenases, COX1 (PTGS1) and COX2 (PTGS2), and four downstream enzymes of the COX/prostaglandin pathway - PTGS3 (PTGDS), PTGES1, PTGES2 and PTGES3 - in invasive breast cancer. The Clinical Proteomic Tumor Analysis Consortium database was used to determine the expression of these six genes at the protein level. Existing single-cell RNA sequencing data were used to evaluate the expression of the six COX/PG genes in luminal and basal epithelial cells from normal breast tissues. Cox regression Kaplan-Meier adjusted survival analyses were performed to evaluate the association of COX/PG pathway genes in overall survival using the TCGA data. Finally, we utilized the Tumor Immune Estimation Resource to correlate the expression of these six COX/PG genes with tumor infiltrating immune cell number.

RESULTS:

COX1, COX2 and PTGES3 were significantly upregulated at the protein level in breast cancer compared to normal tissues (P < 0.005). However, only PTGES3 expression was elevated at both the mRNA and protein level in breast cancer (P < 0.0005). PTGES3 is the most highly expressed enzymes within the COX/PG pathway in both luminal and basal epithelial cells in normal breast tissues. Using Cox Regression Kaplan-Meier survival analysis, PTGES3 expression had a significant inverse prognostic association with breast cancer survival [HR >1.43, P = 0.0057]. Elevated PTGES3 expression within the tumor microenvironment significantly correlated with CD8+ T cell abundance, suggesting a possible immunomodulatory role of PTGES3 in the tumor microenvironment.

CONCLUSIONS:

PTGES3, a terminal synthetase in the COX/prostaglandin pathway, is a putative prognostic marker in breast cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Prostaglandina-E Sintases Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Prostaglandina-E Sintases Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article