The Suprabasal Expression of α6ß4 Integrin Is Associated with a High Risk for Malignant Progression in Mouse Skin Carcinogenesis

Tamar Tennenbaum, Arin K. Weiner, Adam J. Belanger, Adam B. Glick, Henry Hennings, Stuart H. Yuspa

Research output: Contribution to journalArticlepeer-review

116 Scopus citations

Abstract

Enhanced expression of the β4 integrin complex has been linked to malignant progression in mouse skin carcinogenesis. To determine if α6β4 expression can predict risk for malignant conversion among populations of benign skin tumors, we analyzed the distribution of o604 and other markers of profession in papillomas at high and low risk for malignant progression. After initiation with 7,12-dimethylbenz[a]anthracene, mice were promoted with 12-O-tetradecanoylphorbol-13-acetate to induce predominantly low risk tumors or promoted with mezerein to produce predominantly high risk tumors. When tumors first appeared at 8 weeks after promotion, high risk papillomas demonstrated basal and suprabasal α6β4 expression, loss of keratin 1, and aberrant expression of keratin 13. In these tumors α6β4 expression coincided with an expansion of the proliferating compartment as indicated by suprabasal bromodeoxyuridine labeling. In contrast, α6β4 immunostaining was confined to basal cells in low risk tumors, keratin 1 was abundant, and keratin 13 was absent in the majority of this group, while proliferating cells were largely in the basal compartment By 33 weeks, α6β4 suprabasal expression continued to distinguish groups at higher risk for malignant conversion, but keratin 13 was expressed in all groups. At this time, high risk tumors displayed focal expression of keratin 8 and y-glutamyltranspeptidase, markers also found in chemically induced carcinomas. Keratin 8 and γ-glutamyltranspeptidase were expressed only in α6β4 positive cells. These results indicate that expression of α6β4 integrin in suprabasal strata serves as an early predictive marker to identify benign squamous tumors at high risk for malignant progression.

Original languageEnglish (US)
Pages (from-to)4803-4810
Number of pages8
JournalCancer Research
Volume53
Issue number20
StatePublished - Oct 1993

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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