Differential roles of STAT3 in the initiation and growth of lung cancer.

Abstract

Signal transducer and activator of transcription 3 (STAT3) is linked to multiple cancers, including pulmonary adenocarcinoma. However, the role of STAT3 in lung cancer pathogenesis has not been determined. Using lung epithelial-specific inducible knockout strategies, we demonstrate that STAT3 has contrasting roles in the initiation and growth of both chemically and genetically induced lung cancers. Selective deletion of lung epithelial STAT3 in mice before cancer induction by the smoke carcinogen, urethane, resulted in increased lung tissue damage and inflammation, K-Ras oncogenic mutations and tumorigenesis. Deletion of lung epithelial STAT3 after establishment of lung cancer inhibited cancer cell proliferation. Simultaneous deletion of STAT3 and expression of oncogenic K-Ras in mouse lung elevated pulmonary injury, inflammation and tumorigenesis, but reduced tumor growth. These studies indicate that STAT3 prevents lung cancer initiation by maintaining pulmonary homeostasis under oncogenic stress, whereas it facilitates lung cancer progression by promoting cancer cell growth. These studies also provide a mechanistic basis for targeting STAT3 to lung cancer therapy.

• Authors: Jingjiao Zhou, Zhaoxia Qu, Shapei Yan, Fan Sun, Jeffrey A Whitsett, Steven D Shapiro, Gutian Xiao
• Journal: Oncogene (Oncogene) Vol. 34 Issue 29 Pg. 3804-3814 (Jul 2015) ISSN: 1476-5594 [Electronic] England
• PMID: 25284582 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• STAT3 Transcription Factor
• Urethane
• Hras protein, mouse
• Proto-Oncogene Proteins p21(ras)

Topics

• Animals
• Cell Proliferation (genetics)
• Cell Transformation, Neoplastic (genetics, metabolism)
• Cells, Cultured
• Gene Expression Regulation, Neoplastic
• Immunoblotting
• Immunohistochemistry
• Lung (metabolism, pathology)
• Lung Neoplasms (chemically induced, genetics, metabolism)
• Mice, Knockout
• Mice, Transgenic
• Mutation
• Pneumonia (chemically induced, genetics, metabolism)
• Proto-Oncogene Proteins p21(ras) (genetics, metabolism)
• Reverse Transcriptase Polymerase Chain Reaction
• STAT3 Transcription Factor (genetics, metabolism)
• Tumor Burden (genetics)
• Urethane