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The role of PDGF-B/PDGFR-BETA axis in the normal development and carcinogenesis of the breast
- Source :
- Critical Reviews in Oncology/Hematology. 131:46-52
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- PDGFs/PDGFRs axis is documented as an important tumor-promoting agent and potential therapeutic target for several human carcinomas, including breast cancer. However, little is known about the role played by the PDGF family members in the normal development of the breast tissue, breast carcinogenesis and tumor-microenvironment dynamics Despite its potent pro-lymphangiogenic effects, PDGF-B/PDGFR-beta axis remains controversial and incompletely elucidated in the field of breast cancer, with emphasis to its differential implications in breast cancer molecular subtypes. Although some data are available concerning this aspect, little or no information is found regarding the role of the PDGF-B/PDGFR-beta axis in rare and aggressive types of breast cancers, such as triple negative breast cancers (TNBCs) and its associated subtypes This review attempted to gather as many data as possible concerning PDGFs family members in the normal breast tissue and in breast carcinogenesis with special focus on their role in diagnosis and therapeutic approach.
- Subjects :
- 0301 basic medicine
Carcinogenesis
medicine.medical_treatment
Breast Neoplasms
medicine.disease_cause
Targeted therapy
Receptor, Platelet-Derived Growth Factor beta
03 medical and health sciences
Therapeutic approach
0302 clinical medicine
Breast cancer
Tumor Microenvironment
Animals
Humans
Medicine
Breast
skin and connective tissue diseases
PDGFR beta
Triple negative
Tumor microenvironment
business.industry
Proto-Oncogene Proteins c-sis
Hematology
medicine.disease
030104 developmental biology
Oncology
030220 oncology & carcinogenesis
Cancer research
Female
business
Normal breast
Subjects
Details
- ISSN :
- 10408428
- Volume :
- 131
- Database :
- OpenAIRE
- Journal :
- Critical Reviews in Oncology/Hematology
- Accession number :
- edsair.doi.dedup.....46cf7e22c1b9ccda12126b483ab205b9
- Full Text :
- https://doi.org/10.1016/j.critrevonc.2018.08.002