Decreased expression of the DCC gene in human breast carcinoma
Surgery Today, ISSN: 0941-1291, Vol: 26, Issue: 11, Page: 900-903
1996
- 8Citations
- 8Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef5
- Captures8
- Readers8
Article Description
Inactivation of the 'deleted in colon cancer' (DCC) gene on chromosome 18 is known to be associated with the tumorigenesis and metastasis of colorectal cancer. In the present study, we investigated the expression of DCC and the c-erbB-2 product in surgical specimens from 45 patients with breast cancer by immunohistochemical staining, and found the expression of DCC to be decreased in 23 (51%) tumors. In 8 years of follow-up, 11 of 22 (50%) patients with DCC-positive staining tumors, and 17 of 23 (74%) patients with DCC-negative tumors developed recurrence. The stratified analysis, according to the status of axillary lymph node metastasis, showed the same tendency. Overexpression of erbB-2 was detected in 13 (29%) of the 45 breast cancer specimens, but there were no differences in the relapse rate between patients with erbB-2 positive and those with erbB-2 negative tumors. Although the individual alteration of DCC or erbB-2 did not possess independent prognostic significance for the prediction of recurrence, patients with tumors having the double alteration of DCC-negative and erbB. 2-positive showed adverse relapse-free survival (0.025 < P < 0.05). These findings suggest that a decrease in DCC expression and erbB-2 overexpression may influence the progression of breast carcinoma.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0029860647&origin=inward; http://dx.doi.org/10.1007/bf00311792; http://www.ncbi.nlm.nih.gov/pubmed/8931221; http://link.springer.com/10.1007/BF00311792; http://www.springerlink.com/index/pdf/10.1007/BF00311792; http://www.springerlink.com/index/10.1007/BF00311792; https://dx.doi.org/10.1007/bf00311792; https://link.springer.com/article/10.1007/BF00311792
Springer Nature
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