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  • 1
    ISSN: 1569-8041
    Keywords: breast carcinoma ; high performance liquid chromatography ; lymph node metastasis ; pyrimidine nucleoside phosphorylase ; reverse transcriptase-polymerase chain reaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background: The clinical significance of pyrimidine nucleoside phosphorylase (PyNPase) activity in breast carcinomas has never been determined. Materials and methods: In 41 cases of breast carcinoma, the enzyme activity of PyNPase was determined by the high performance liquid chromatography (HPLC) assay and its value was analyzed with clinicopathologic variables. The expression level of mRNA was examined by the semi-quantitative reverse transcriptase-polymerase chain reaction (RT–PCR) assay and compared with the enzyme activity. Results: The higher activity of PyNPase was significantly correlated not only with the presence of vascular permeation (P = 0.02) but of lymph node metastasis (P = 0.02). The mRNA expression correlated well with the enzyme activity (r = 0.74, P 〈 0.01). A multivariate analysis disclosed the PyNPase factor to be associated with lymph node metastasis. In addition, 17 (41%) showed positive staining only in the tumor stromal cells and 18 (44%) cases showed positive staining in both the tumor stromal cells and the carcinoma cells by immunohistochemical study. Conclusions: These findings suggest that PyNPase activity is a new marker predicting the malignant potential of breast carcinomas, especially with respect to lymph node metastasis, and that the RT–PCR assay is a more useful method than direct evaluation of PyNPase activity.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1569-8041
    Keywords: adjuvant therapy ; breast cancer ; second cancer ; tamoxifen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background:Women treated with tamoxifen for breast cancer are atincreased risk of endometrial cancer. We conducted a retrospective cohortstudy to evaluate the risk of second primary cancers after adjuvant tamoxifentherapy for breast cancer in Japan. Patients and methods:The subjects of the study were 6148 womenwho had been diagnosed with stage I, II, or IIIA unilateral primary breastcancer and had received surgical treatment during the period from January 1982through December 1990 at nine institutions in Japan. The information on eachpatient was obtained from medical records or a prospectively compiled computerdatabase at each institution. Results:Of the 6148 women, 3588 (58.4%) were administeredtamoxifen as an adjuvant treatment and 2560 (41.6%) were notadministered. Median follow-up periods were 7.64 years for tamoxifen-treatedpatients and 8.10 years for non-tamoxifen-treated patients, respectively. Theduration of tamoxifen treatment was mostly two years or less (80.7%),and few patients received tamoxifen for more than five years. The cumulativeincidence rates of all second cancers at 10 years were 4.61% and4.09% among tamoxifen-treated and non-tamoxifen-treated patients(P = 0.62), respectively, and the incidence rate ratio (IRR) forall second cancers was 1.06 (95% confidence interval (CI):0.77–1.47) after adjustment of several covariates. The numbers ofendometrial cancers was 9 and 3 among tamoxifen-treated andnon-tamoxifen-treated patients, respectively, and the IRR was 2.37 (95%CI: 0.64–8.77, P = 0.20). Of the 12 patients who developedendometrial cancer, 4 died of cancer (for 3 of them, the cause of death wasbreast cancer), and the other 8 patients were alive as of March 1996. Stomachcancer was the most frequent second cancer and the IRR was 1.34 (95%CI: 0.76–2.38, P = 0.31). There was no substantialincrease in any other type of gastrointestinal cancer such as colorectal andliver cancers among tamoxifen-treated patients. Conclusions:The incidence and risk of second primary cancersassociated with tamoxifen therapy is low. The potential benefit of adjuvanttamoxifen therapy in breast cancer patients outweighs the risk of secondprimary cancers for Japanese breast cancer patients.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Annals of oncology 8 (1997), S. 369-372 
    ISSN: 1569-8041
    Keywords: BAGE ; MAGE ; specific immunotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background: The MAGE and BAGE genes code for distinct antigens, which arerecognized on melanoma cells as well as on other various tumor cells byautologous cytolytic T lymphocytes. These antigens may thus constitute usefultargets for specific immunotherapy, since no expression of MAGE or BAGE geneshas been recognized in normal tissue except for the testis. Patients and methods: We studied the MAGE-1, MAGE-3, and BAGE geneexpression observed in 49 Japanese breast cancers. Gene expression wasevaluated by reverse transcription polymerase chain reaction. Results: Out of 49 tumor tissue specimens of primary breast cancers, theexpression of MAGE-1, -3 and BAGE was recognized in 15 (31%), 12(24%), and 4 (8%) tumors, respectively. The expression of MAGEand BAGE genes is not recognized in normal breast tissue. The expression ofthe MAGE-3 gene was frequently recognized in tumors with lymphatic and/orvascular vessel permeations. Either MAGE-1 or -3 gene expressions were inducedin 1 of 3 MAGE-1 negative breast cell lines or 1 of 3 MAGE-3 negative breastcell lines by the treatment with 5-aza-2′-deoxycytidine. Conclusions: These findings suggest that: 1) the identification of suchantigens coded by MAGE or BAGE genes may thus offer the possibility of usingspecific immunotherapy, and 2) the use of a demethylating agent may increasethe number of patients who might be candidates for MAGE specificimmunotherapy.
    Type of Medium: Electronic Resource
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