Recombinant Human Granulocyte Colony-Stimulating Factor Promotes Preinvasive and Invasive Estrogen Receptor-Positive Tumor Development in MMTV-erbB2 Mice.
10.4048/jbc.2015.18.2.126
- Author:
Chun Ling ZHAO
1
;
Guang Ping ZHANG
;
Zheng Zheng XIAO
;
Zhi Kun MA
;
Cai Peng LEI
;
Shi Yuan SONG
;
Ying Ying FENG
;
Ya Chao ZHAO
;
Xiao Shan FENG
Author Information
1. Department of Oncology, Cancer Institute, First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China. fengxiaoshan2014@163.com
- Publication Type:In Vitro ; Original Article
- Keywords:
Carcinogenesis;
Cell proliferation;
Granulocyte colony-stimulating factor;
Mammary gland
- MeSH:
Animals;
Breast Neoplasms;
Carcinogenesis;
Cell Proliferation;
Estrogens*;
Granulocyte Colony-Stimulating Factor*;
Humans;
Immunohistochemistry;
Injections, Subcutaneous;
Mammary Glands, Human;
Mammary Tumor Virus, Mouse;
Mice*;
Polymerase Chain Reaction;
Proliferating Cell Nuclear Antigen;
Reverse Transcription;
Transducers
- From:Journal of Breast Cancer
2015;18(2):126-133
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: We investigated whether recombinant human granulocyte colony-stimulating factor (rhG-CSF) could promote the development of preinvasive and invasive breast cancer in mouse mammary tumor virus (MMTV-erbB2) mice with estrogen receptor-positive tumors. METHODS: MMTV-erbB2 mice were randomly divided into three experimental groups with 20 mice in each group. MMTV-erbB2 mice were treated with daily subcutaneous injections of vehicle or rhG-CSF (low-rhG-CSF group, rhG-CSF 0.125 microg; vehicle-rhG-CSF group, normal saline 0.25 microg; and high-rhG-CSF group, rhG-CSF 0.25 microg) at 3 months of age. Cellular and molecular mechanisms of G-CSF action in mammary glands were investigated via immunohistochemistry and reverse transcription polymerase chain reaction. RESULTS: Low, but not high, rhG-CSF doses significantly accelerated mammary tumorigenesis in MMTV-erbB2 mice. Short-term treatment with rhG-CSF could significantly promote the development of preinvasive mammary lesions. The cancer prevention effect was associated with reduced expression of proliferating cell nuclear antigen, cluster of differentiation 34, and signal transducers and activators of transcription 3 in mammary glands by >80%. CONCLUSION: We found that G-CSF was regulated by rhG-CSF both in vitro and in vivo. Identification of G-CSF genes helped us further understand the mechanism by which G-CSF promotes cancer. Low doses of rhG-CSF could significantly increase tumor latency and increase tumor multiplicity and burden. Moreover, rhG-CSF effectively promotes development of both malignant and premalignant mammary lesions in MMTV-erbB2 mice.
