Abstract |
Annexin I protein expression was evaluated in patient-matched longitudinal study sets of laser capture microdissected normal, premalignant, and invasive epithelium from human esophageal squamous cell cancer and prostatic adenocarcinoma. In 25 esophageal cases (20 by Western blot and 5 by immunohistochemistry) and 17 prostate cases (3 by Western blot and 14 by immunohistochemistry), both tumor types showed either complete loss or a dramatic reduction in the level of annexin I protein expression compared with patient-matched normal epithelium (P < or = 0.05). Moreover, by using Western blot analysis of laser capture microdissected, patient-matched longitudinal study sets of both tumor types, the loss of protein expression occurred in premalignant lesions. Concordance of this result with immunohistochemical analysis suggests that annexin I may be an essential component for maintenance of the normal epithelial phenotype. Additional studies investigating the mechanism(s) and functional consequences of annexin I protein loss in tumor cells are warranted.
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Authors | C P Paweletz, D K Ornstein, M J Roth, V E Bichsel, J W Gillespie, V S Calvert, C D Vocke, S M Hewitt, P H Duray, J Herring, Q H Wang, N Hu, W M Linehan, P R Taylor, L A Liotta, M R Emmert-Buck, E F Petricoin 3rd |
Journal | Cancer research
(Cancer Res)
Vol. 60
Issue 22
Pg. 6293-7
(Nov 15 2000)
ISSN: 0008-5472 [Print] United States |
PMID | 11103786
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Adenocarcinoma
(metabolism)
- Annexin A1
(biosynthesis, metabolism)
- Blotting, Western
- Carcinoma, Squamous Cell
(metabolism)
- Dissection
(methods)
- Epithelium
(metabolism)
- Esophageal Neoplasms
(metabolism)
- Esophagus
(metabolism)
- Humans
- Immunohistochemistry
- Longitudinal Studies
- Male
- Precancerous Conditions
(metabolism)
- Prostate
(metabolism)
- Prostatic Neoplasms
(metabolism)
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