Molecular transitions from papillomavirus infection to cervical precancer and cancer Role of stromal estrogen receptor signaling

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 112; no. 25; pp. E3255 - E3264
• Main Authors: den Boon, Johan A., Pyeon, Dohun, Wang, Sophia S., Horswill, Mark, Schiffman, Mark, Sherman, Mark, Zuna, Rosemary E., Wang, Zhishi, Hewitt, Stephen M., Pearson, Rachel, Schott, Meghan, Chung, Lisa, He, Qiuling, Lambert, Paul, Walker, Joan, Newton, Michael A., Wentzensen, Nicolas, Ahlquist, Paul
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 23-06-2015; National Acad Sciences
• Series: PNAS Plus
• Subjects: Angiogenesis; Biological Sciences; Cell growth; Cervical cancer; Cervical Intraepithelial Neoplasia - etiology; Cervical Intraepithelial Neoplasia - virology; Deoxyribonucleic acid; Disease Progression; DNA; Estrogen Receptor alpha - genetics; Estrogen Receptor alpha - metabolism; Female; Gene expression; Gene Expression Profiling; Human papillomavirus; Humans; Papillomavirus Infections - pathology; PNAS Plus; Signal Transduction; Stromal Cells - metabolism; Uterine Cervical Neoplasms - etiology; Uterine Cervical Neoplasms - virology; estrogen; tumor microenvironment; cervical cancer; stroma; HPV
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1509322112

To study the multistep process of cervical cancer development, we analyzed 128 frozen cervical samples spanning normalcy, increasingly severe cervical intraepithelial neoplasia (CIN1–CIN3), and cervical cancer (CxCa) from multiple perspectives, revealing a cascade of progressive changes.Compared with normal tissue, expression of many DNA replication/repair and cell proliferation genes was increased in CIN1/CIN2 lesions and further sustained in CIN3, consistent with high-risk human papillomavirus (HPV)-induced tumor suppressor inactivation. The CIN3-to-CxCa transition showed metabolic shifts, including decreased expression of mitochondrial electron transport complex components and ribosomal protein genes. Significantly, despite clinical, epidemiological, and animal model results linking estrogen and estrogen receptor alpha (ERα) to CxCa, ERα expression declined >15-fold from normalcy to cancer, showing the strongest inverse correlation of any gene with the increasing expression of p16, a marker for HPV-linked cancers. This drop in ERα in CIN and tumor cells was confirmed at the protein level. However, ERα expression in stromal cells continued throughout CxCa development. Our further studies localized stromal ERα to FSP1+, CD34+, SMA− precursor fibrocytes adjacent to normal and precancerous CIN epithelium, and FSP1−, CD34−, SMA+ activated fibroblasts in CxCas. Moreover, rank correlations with ERα mRNA identified IL-8, CXCL12, CXCL14, their receptors, and other angiogenesis and immune cell infiltration and inflammatory factors as candidates for ERα-induced stroma–tumor signaling pathways. The results indicate that estrogen signaling in cervical cancer has dramatic differences from ERα+ breast cancers, and imply that estrogen signaling increasingly proceeds indirectly through ERα in tumor-associated stromal fibroblasts.