» Articles » PMID: 29286323

Fibrocytes: A Novel Stromal Cells to Regulate Resistance to Anti-Angiogenic Therapy and Cancer Progression

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2017 Dec 30
PMID 29286323
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

An adequate blood supply is essential for cancer cells to survive and grow; thus, the concept of inhibiting tumor angiogenesis has been applied to cancer therapy, and several drugs are already in clinical use. It has been shown that treatment with those anti-angiogenic drugs improved the response rate and prolonged the survival of patients with various types of cancer; however, it is also true that the effect was mostly limited. Currently, the disappointing clinical results are explained by the existence of intrinsic or acquired resistance to the therapy mediated by both tumor cells and stromal cells. This article reviews the mechanisms of resistance mediated by stromal cells such as endothelial cells, pericytes, fibroblasts and myeloid cells, with an emphasis on fibrocytes, which were recently identified as the cell type responsible for regulating acquired resistance to anti-angiogenic therapy. In addition, the other emerging role of fibrocytes as mediator-producing cells in tumor progression is discussed.

Citing Articles

Precision Medicine for Metastatic Colorectal Cancer: Where Do We Stand?.

Underwood P, Pawlik T Cancers (Basel). 2024; 16(22).

PMID: 39594824 PMC: 11593240. DOI: 10.3390/cancers16223870.


Lung cancer organoids: models for preclinical research and precision medicine.

Liu Y, Zhou Y, Chen P Front Oncol. 2023; 13:1293441.

PMID: 37941550 PMC: 10628480. DOI: 10.3389/fonc.2023.1293441.


Resistance to targeted therapy in metastatic colorectal cancer: Current status and new developments.

Tang Y, Li D, Duan J, Sheng L, Wang X World J Gastroenterol. 2023; 29(6):926-948.

PMID: 36844139 PMC: 9950860. DOI: 10.3748/wjg.v29.i6.926.


Analysis of the chemotactic factors for tumor-infiltrating fibrocytes and their prognostic significances in lung cancer.

Tobiume M, Mitsuhashi A, Saijo A, Ogino H, Afroj T, Ogawa H Oncol Lett. 2022; 24(5):417.

PMID: 36245829 PMC: 9555093. DOI: 10.3892/ol.2022.13537.


Blockade of PD-1/PD-L1 Pathway Enhances the Antigen-Presenting Capacity of Fibrocytes.

Afroj T, Mitsuhashi A, Ogino H, Saijo A, Otsuka K, Yoneda H J Immunol. 2021; 206(6):1204-1214.

PMID: 33504617 PMC: 7939041. DOI: 10.4049/jimmunol.2000909.


References
1.
Al-Abd A, Alamoudi A, Abdel-Naim A, Neamatallah T, Ashour O . Anti-angiogenic agents for the treatment of solid tumors: Potential pathways, therapy and current strategies - A review. J Adv Res. 2017; 8(6):591-605. PMC: 5544473. DOI: 10.1016/j.jare.2017.06.006. View

2.
Gomperts B, Strieter R . Fibrocytes in lung disease. J Leukoc Biol. 2007; 82(3):449-56. DOI: 10.1189/jlb.0906587. View

3.
Vasudev N, Reynolds A . Anti-angiogenic therapy for cancer: current progress, unresolved questions and future directions. Angiogenesis. 2014; 17(3):471-94. PMC: 4061466. DOI: 10.1007/s10456-014-9420-y. View

4.
Valkovic T, Dobrila F, Melato M, Sasso F, Rizzardi C, Jonjic N . Correlation between vascular endothelial growth factor, angiogenesis, and tumor-associated macrophages in invasive ductal breast carcinoma. Virchows Arch. 2002; 440(6):583-8. DOI: 10.1007/s004280100458. View

5.
Laurent J, Touvrey C, Botta F, Kuonen F, Ruegg C . Emerging paradigms and questions on pro-angiogenic bone marrow-derived myelomonocytic cells. Int J Dev Biol. 2011; 55(4-5):527-34. DOI: 10.1387/ijdb.103228jl. View