» Articles » PMID: 36831623

Interactions Between Platelets and Tumor Microenvironment Components in Ovarian Cancer and Their Implications for Treatment and Clinical Outcomes

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2023 Feb 25
PMID 36831623
Authors
Affiliations
Soon will be listed here.
Abstract

Platelets, the primary operatives of hemostasis that contribute to blood coagulation and wound healing after blood vessel injury, are also involved in pathological conditions, including cancer. Malignancy-associated thrombosis is common in ovarian cancer patients and is associated with poor clinical outcomes. Platelets extravasate into the tumor microenvironment in ovarian cancer and interact with cancer cells and non-cancerous elements. Ovarian cancer cells also activate platelets. The communication between activated platelets, cancer cells, and the tumor microenvironment is via various platelet membrane proteins or mediators released through degranulation or the secretion of microvesicles from platelets. These interactions trigger signaling cascades in tumors that promote ovarian cancer progression, metastasis, and neoangiogenesis. This review discusses how interactions between platelets, cancer cells, cancer stem cells, stromal cells, and the extracellular matrix in the tumor microenvironment influence ovarian cancer progression. It also presents novel potential therapeutic approaches toward this gynecological cancer.

Citing Articles

Correlation Between Intravascular Platelet Aggregation in Tumors and Hypoxia-Inducible Factor 1 Alpha Expression in Epithelial Ovarian Cancer: Implications for Prognosis and Staging.

Ryu J, Jeong Y, Lee S, Choi Y Cancers (Basel). 2025; 17(3).

PMID: 39941717 PMC: 11815719. DOI: 10.3390/cancers17030345.


Clinically relevant body composition phenotypes are associated with distinct circulating cytokine and metabolomic milieus in epithelial ovarian cancer patients.

Davis E, Hsiao H, Barone N, Rosario S, Cannioto R Front Immunol. 2024; 15:1419257.

PMID: 39575261 PMC: 11578747. DOI: 10.3389/fimmu.2024.1419257.


Plasma microRNA Environment Linked to Tissue Factor Pathway and Cancer-Associated Thrombosis: Prognostic Significance in Ovarian Cancer.

Tavares V, Savva-Bordalo J, Rei M, Liz-Pimenta J, Assis J, Pereira D Biomolecules. 2024; 14(8).

PMID: 39199316 PMC: 11352941. DOI: 10.3390/biom14080928.


Haemostatic Gene Expression in Cancer-Related Immunothrombosis: Contribution for Venous Thromboembolism and Ovarian Tumour Behaviour.

Tavares V, Savva-Bordalo J, Rei M, Liz-Pimenta J, Assis J, Pereira D Cancers (Basel). 2024; 16(13).

PMID: 39001418 PMC: 11240748. DOI: 10.3390/cancers16132356.

References
1.
Meikle C, Meisler A, Bird C, Jeffries J, Azeem N, Garg P . Platelet-T cell aggregates in lung cancer patients: Implications for thrombosis. PLoS One. 2020; 15(8):e0236966. PMC: 7416940. DOI: 10.1371/journal.pone.0236966. View

2.
Kehrl J, Thevenin C, Rieckmann P, Fauci A . Transforming growth factor-beta suppresses human B lymphocyte Ig production by inhibiting synthesis and the switch from the membrane form to the secreted form of Ig mRNA. J Immunol. 1991; 146(11):4016-23. View

3.
Sun C, Feng S, Cao Z, Bei J, Chen Q, Zhao W . Up-Regulated Expression of Matrix Metalloproteinases in Endothelial Cells Mediates Platelet Microvesicle-Induced Angiogenesis. Cell Physiol Biochem. 2017; 41(6):2319-2332. DOI: 10.1159/000475651. View

4.
Giraldo N, Sanchez-Salas R, Peske J, Vano Y, Becht E, Petitprez F . The clinical role of the TME in solid cancer. Br J Cancer. 2018; 120(1):45-53. PMC: 6325164. DOI: 10.1038/s41416-018-0327-z. View

5.
Arango Duque G, Descoteaux A . Macrophage cytokines: involvement in immunity and infectious diseases. Front Immunol. 2014; 5:491. PMC: 4188125. DOI: 10.3389/fimmu.2014.00491. View