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  • Cheng, Ya-Wen  (6)
  • Hsu, Nan-Yung  (6)
  • 1
    In: The Annals of Thoracic Surgery, Elsevier BV, Vol. 95, No. 4 ( 2013-4), p. 1196-1203
    Type of Medium: Online Resource
    ISSN: 0003-4975
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2013
    detail.hit.zdb_id: 211007-6
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  • 2
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2012
    In:  Cancer Research Vol. 72, No. 8_Supplement ( 2012-04-15), p. 1187-1187
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 72, No. 8_Supplement ( 2012-04-15), p. 1187-1187
    Abstract: Background. A polymorphism at codon 72 of the p53 tumor suppressor gene is a possible determinant for cancer risk, particularly for carcinomas associated with HPV infection. We recently reported that high-risk HPV 16/18 E6 protein was associated with p53 protein degradation in lung cancer. The present study addressed the relationship between the different p53 genotypes and HPV oncoprotein expression with respect to p53 protein degradation in 319 primary lung cancer patients. Methods. The p53 codon 72 polymorphisms, HPV 16/18 infection, HPV 16/18 E6 and p53 protein expression were determined for all patients by PCR-RFLP, nested-PCR and immunohistochemical analysis. Results. The presence of HPV 16/18 DNA and E6 protein was inversely correlated with p53 expression. The frequency of p53 protein degradation in HPV 16/18 E6-positive/Arg/Arg lung cancer tumours was also much higher than in the HPV 16/18 E6-negative/Arg/Arg, HPV 16/18 E6-positive/Arg/pro+pro/pro, and HPV 16/18 E6-negative/Arg/pro+pro/pro groups. After adjusting for polymorphism, HPV 16/18 E6 protein, HPV 16/18 DNA, gender, smoking habit and tumor type, the major contributors to p53 degradation in lung cancer patients were p53 codon72 polymorphism and HPV 16/18 E6 oncoprotein expression. This correlation was not found for HPV 16/18 DNA infection. Conclusion. These results suggested that the involvement of HPV 16/18 E6 protein in the p53 inactivation that contributes to HPV-infected lung tumourigenesis is correlated with the p53 codon 72 genotype. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 1187. doi:1538-7445.AM2012-1187
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2012
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
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  • 3
    In: Surgery, Elsevier BV, Vol. 160, No. 6 ( 2016-12), p. 1591-1598
    Type of Medium: Online Resource
    ISSN: 0039-6060
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 202467-6
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  • 4
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2014
    In:  Cancer Research Vol. 74, No. 19_Supplement ( 2014-10-01), p. 1470-1470
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 74, No. 19_Supplement ( 2014-10-01), p. 1470-1470
    Abstract: Objective: Over the last decade, the incidence of breast cancer increased year by year, and the mortality rate is the top of female cancer in Taiwan. Previous study showed that overexpression of miR-21 was associated with recurrence in breast cancer. The aim of this study was to analyze the association of miR-21 expression and clinic pathologic data and to investigate whether the effect of miR-21 through PTEN pathway. Materials and Methods: A total of 120 female breast cancer patients, who were enrolled at a single medical center in Taichung. MiR-21, PTEN, hormone receptor (estrogen receptor,progesterone receptor) and HER-2 (human Epidermal Growth Factor Receptor 2) receptor were analyzed by quantitative RT-PCR. The function of invasion and migration of four breast cancer cell lines (T-47D, MDA-MB-231, MCF-7 and BT-474) were analyzed by invasion and migration assay and wound healing assay. Results: Our data showed that no significantly difference was found between miR-21 and PTEN. MiR-21 expression was positive correlated with HER-2/neu mRNA levels (P=0.038). Patients with high miR-21 level had poor disease-free survival (p=0.047) compared with low miR-21 level patients. In addition, patients with high PTEN level had poor disease-free survival (P=0.024). We also found that patients with miR-21 high/ HER-2/neu high or miR-21 high/ PTEN high had poor disease-free survival (miR-21/HER-2/neu, p=0.009; miR-21/PTEN, p=0.003). Thus, we suggested that the expressions of miR-21, HER-2/neu and PTEN play important roles in prognosis and associated with recurrence in breast cancer. These results were also confirmed in cell model experiments. Conclusion: In this study, we found that the expression of miR-21, HER-2/neu, and PTEN were associated with the recurrence of breast cancer in Taiwan. Thus, we suggested that the other pathways maybe involved in miR-21 mediated pathogenesis of breast cancer. Citation Format: Hsiao-Ching Lin, Ya-Wen Cheng, Nan-Yung Hsu. The association of miR-21, HER-2/neu, and PTEN expression and clinical outcome of breast cancer. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 1470. doi:10.1158/1538-7445.AM2014-1470
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2014
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
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  • 5
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2010
    In:  Cancer Research Vol. 70, No. 8_Supplement ( 2010-04-15), p. 1862-1862
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 70, No. 8_Supplement ( 2010-04-15), p. 1862-1862
    Abstract: A polymorphism at codon 72 of the p53 tumor suppressor gene is as a possible determinant for cancer risk and particularly carcinomas associated with HPV infection. Our recent report has shown that high-risk HPV 16/18 E6 proteins were associated with p53 protein degradation in lung cancer. To address the relationship of the different p53 genotypes and HPV oncoprotein expression in p53 protein degradation of lung cancer, 141 primary lung cancer patients were included in this study. PCR-RFLP, nested-PCR and immunohistochemial analysis were used to detect the p53 codon 72 polymorphism, HPV 16/18 infection, HPV 16/18 E6 and p53 protein expression. Our data showed that HPV 16/18 E6 protein but not HPV 16/18 DNA were reversely correlated with p53 expression, which was further confirmed by tissue in situ immunostaining. Additionally, the frequency of p53 protein negative expression in HPV 16/18 E6-positive/Arg homozygosity lung cancer tumors is much higher than that in the other three categorizes. This correlation was not found in HPV DNA infection. In conclusion, HPV 16/18 E6 proteins involvement in p53 inactivation to contribute to HPV-infected lung tumorigenesis is correlated with p53 codon 72 genotypes. Note: This abstract was not presented at the AACR 101st Annual Meeting 2010 because the presenter was unable to attend. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 17-21; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2010;70(8 Suppl):Abstract nr 1862.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2010
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
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  • 6
    Online Resource
    Online Resource
    Impact Journals, LLC ; 2016
    In:  Oncotarget Vol. 7, No. 15 ( 2016-04-12), p. 19850-19862
    In: Oncotarget, Impact Journals, LLC, Vol. 7, No. 15 ( 2016-04-12), p. 19850-19862
    Type of Medium: Online Resource
    ISSN: 1949-2553
    URL: Issue
    Language: English
    Publisher: Impact Journals, LLC
    Publication Date: 2016
    detail.hit.zdb_id: 2560162-3
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