Upregulation and redistribution of integrin α6β4 expression occurs at an early stage in pancreatic adenocarcinoma progression

Zobeida Cruz-Monserrate, Suimin Qiu, B. Mark Evers, Kathleen L. O'Connor

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

Pancreatic adenocarcinomas are highly invasive cancers for reasons that are currently unclear. Here we sought to determine if the proinvasive integrin α6β4 may be related to pancreatic adenocarcinoma tumor progression. Expression of integrin α6β4 was analyzed via immunohistochemistry for the β4 subunit in normal pancreas, pancreatic intraepithelial neoplasia (PanIN) lesions, pancreatic adenocarcinomas and chronic pancreatitis. In normal pancreatic ducts, integrin α6β4 was noted only at the cell's basal interface with the basement membrane. In pancreatic adenocarcinomas, 92% (104/113) demonstrated overexpression of integrin α6β4 and altered localization to the cytoplasm and membranous regions. This pattern of expression was observed in all PanIN lesions as early as PanIN-1A, and was evident in lesions that were juxtapositioned to normal epithelium. In contrast, 93% (13/14) of chronic pancreatitis samples resembled the staining pattern of normal pancreas. When cancer was present in areas of chronic pancreatitis, this altered expression of α6β4 integrin identified the cancer. We conclude that integrin α6β4 is expressed only on the basal surface of ductal cells in normal pancreas and chronic pancreatitis. During pancreatic adenocarcinoma progression, the α6β4 integrin is dramatically overexpressed and displays altered localization at the earliest stages of PanIN, thus representing an early event in pancreatic adenocarcinoma progression.

Original languageEnglish
Pages (from-to)656-667
Number of pages12
JournalModern Pathology
Volume20
Issue number6
DOIs
StatePublished - Jun 2007

Bibliographical note

Funding Information:
We gratefully acknowledge Linda E Muehlberger for her help in troubleshooting the immunohistochemistry method, Dr William Nealon and Dr Jingwu Xie for helpful discussions, Karen Martin for graphics assistance and Dr James Brady for aid with statistical analysis. This work was supported by the National Institutes of Health Grants R21—CA102125 (KLO) and F31 CA106201 (ZCM).

Funding

We gratefully acknowledge Linda E Muehlberger for her help in troubleshooting the immunohistochemistry method, Dr William Nealon and Dr Jingwu Xie for helpful discussions, Karen Martin for graphics assistance and Dr James Brady for aid with statistical analysis. This work was supported by the National Institutes of Health Grants R21—CA102125 (KLO) and F31 CA106201 (ZCM).

FundersFunder number
National Institutes of Health (NIH)R21—CA102125
National Childhood Cancer Registry – National Cancer InstituteF31CA106201

    Keywords

    • Chronic pancreatitis
    • Immunohistochemistry
    • Integrins
    • Pancreatic cancer
    • Pancreatic intraepithelial neoplasia (PanINs)
    • Precursor lesion

    ASJC Scopus subject areas

    • Pathology and Forensic Medicine

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