Origins and actions of tumor necrosis factor α in postmenopausal breast cancer

Tumor necrosis factor α (TNFα) has many roles in both physiological and pathological states. Initially thought to cause necrosis of tumors, research has shown that in many tumor types, including breast cancer, TNFα contributes to growth and proliferation. The presence of TNFα-derived from the tumor and infiltrating immune cells-within a breast tumor microenvironment has been correlated with a more aggressive phenotype, and the postmenopausal ER+ subtype of breast cancers appears to strongly respond to its many pro-growth signaling functions. We discuss how TNFα regulates estrogen biosynthesis within the breast, affecting the activity of the key estrogen-synthesizing enzymes aromatase, estrone sulfatase, and 17β-HSD type 1. Additionally, we describe the anti-adipogenic actions of TNFα that are critical in preventing adjacent estrogen-producing adipose fibroblasts from differentiating, ensuring that the tumor maintains a constant source of estrogen-producing cells. We examine how the increased risk of developing breast cancer in older and obese individuals may be linked to the levels of TNFα in the body. Finally, we evaluate the feasibility of targeting TNFα and its associated pathways as a novel approach to breast cancer therapeutics.

Medienart:

E-Artikel

Erscheinungsjahr:

2013

Erschienen:

2013

Enthalten in:

Zur Gesamtaufnahme - volume:33

Enthalten in:

Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research - 33(2013), 7 vom: 14. Juli, Seite 335-45

Sprache:

Englisch

Beteiligte Personen:

To, Sarah Q [VerfasserIn]
Knower, Kevin C [VerfasserIn]
Clyne, Colin D [VerfasserIn]

Links:

Volltext

Themen:

Antineoplastic Agents
Estrogens
Journal Article
Research Support, Non-U.S. Gov't
Review
Tumor Necrosis Factor-alpha

Anmerkungen:

Date Completed 07.03.2014

Date Revised 11.07.2013

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1089/jir.2012.0155

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM225629542