Abstract | AIMS: METHODS AND RESULTS: Immunohistochemical methods were used to detect TGFbeta-RII in archival breast samples including benign proliferative lesions, ductal carcinoma in situ ( DCIS) and invasive mammary carcinomas (IMC). Neoplastic cells showed reduced expression of TGFbeta-RII in comparison to the normal breast tissue and benign lesions. There was a significant inverse correlation between loss of TGFbeta-RII expression and tumour grade within both DCIS (P = 0.004) and IMC (P = 0.001) groups. There was an inverse correlation between TGFbeta-RII expression and both mitotic count (P = 0.001) and clinical stage (P = 0.004). Oestrogen receptor (P = 0.07) and lymph node status (P = 0.10) were not significantly associated with TGFbeta-RII expression. CONCLUSIONS: These data indicate that decreased expression of TGFbeta-RII may contribute to breast cancer progression and is related to a more aggressive phenotype in both in-situ and invasive carcinomas.
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Authors | H Gobbi, C L Arteaga, R A Jensen, J F Simpson, W D Dupont, S J Olson, P A Schuyler, W D Plummer Jr, D L Page |
Journal | Histopathology
(Histopathology)
Vol. 36
Issue 2
Pg. 168-77
(Feb 2000)
ISSN: 0309-0167 [Print] England |
PMID | 10672063
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Receptors, Transforming Growth Factor beta
- Protein Serine-Threonine Kinases
- Receptor, Transforming Growth Factor-beta Type II
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Breast
(chemistry, pathology)
- Breast Neoplasms
(metabolism, pathology)
- Carcinoma in Situ
(metabolism, pathology)
- Carcinoma, Ductal, Breast
(metabolism, pathology)
- Disease Progression
- Female
- Humans
- Hyperplasia
- Immunohistochemistry
- Middle Aged
- Neoplasm Invasiveness
- Neoplasm Staging
- Protein Serine-Threonine Kinases
- Receptor, Transforming Growth Factor-beta Type II
- Receptors, Transforming Growth Factor beta
(analysis, biosynthesis)
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