Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/43061
DC Field | Value | Language |
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dc.contributor.author | Henríquez-Hernández, Luis Alberto | |
dc.contributor.author | Lloret, Marta | |
dc.contributor.author | Pinar, Beatriz | |
dc.contributor.author | Bordón, Elisa | |
dc.contributor.author | Rey, Agustín | |
dc.contributor.author | Lubrano, Amina | |
dc.contributor.author | Lara, Pedro Carlos | |
dc.date.accessioned | 2018-11-21T12:18:34Z | - |
dc.date.available | 2018-11-21T12:18:34Z | - |
dc.date.issued | 2011 | |
dc.identifier.issn | 0090-8258 | |
dc.identifier.uri | http://hdl.handle.net/10553/43061 | - |
dc.description.abstract | Objectives. To investigate whether BCL-2 expression would improve MVP/IGF-1R prediction of clinical outcome in cervix carcinoma patients treated by radiochemotherapy, and suggest possible mechanisms behind this effect.Methods. Fifty consecutive patients, who achieved complete response to treatment, from a whole series of 60 cases suffering from non-metastatic localized cervical carcinoma, were prospectively included in this study from July 1999 to December 2003. Follow-up was closed in January 2011. All patients received pelvic radiation (45-64.80 Gy in 1.8-2 Gy fractions) with concomitant cisplatin at 40 mg/m2/week closes followed by brachytherapy. Oncoprotein expression was studied by immunohistochemistry in paraffin-embedded tumour tissue.Results. No relation was found between BCL-2 and clinicopathological variables. High MVP/IGF-1R/BCL-2 tumour expression was strongly related to poor local and regional disease-free survival (P < 0.0001), distant disease-free survival (P= 0.010), disease-free survival (P < 0.0001), and cause-specific survival (P < 0.0001). NHEJ repair protein Ku70/80 expression was significantly repressed in tumours overexpressing all three oncoproteins (P= 0.047). No differences were observed in proliferation (Ki67 expression) or P53 alteration.Conclusions. BCL-2, MVP, and IGF-1R overexpression were related to poorer clinical outcome in cervical cancer patients who achieved clinical complete response to radiochemotherapy. The NHEJ repair protein Ku70/80 expression could be involved in the regulation of these oncoproteins. (C) 2011 Elsevier Inc. All rights reserved. | |
dc.publisher | 0090-8258 | |
dc.relation.ispartof | Gynecologic Oncology | |
dc.source | Gynecologic Oncology[ISSN 0090-8258],v. 122, p. 585-589 | |
dc.subject.other | Major Vault Protein | |
dc.subject.other | Adverse Prognostic-Factor | |
dc.subject.other | Squamous-Cell Carcinoma | |
dc.subject.other | Double-Strand Breaks | |
dc.subject.other | End-Joining Pathway | |
dc.subject.other | Down-Regulation | |
dc.subject.other | Dna-Damage | |
dc.subject.other | Repair | |
dc.subject.other | P53 | |
dc.subject.other | Radiotherapy | |
dc.title | BCL-2, in combination with MVP and IGF-1R expression, improves prediction of clinical outcome in complete response cervical carcinoma patients treated by radiochemotherapy | |
dc.type | info:eu-repo/semantics/Article | es |
dc.type | Article | es |
dc.identifier.doi | 10.1016/j.ygyno.2011.05.037 | |
dc.identifier.scopus | 80051550628 | - |
dc.identifier.isi | 000294151200023 | |
dc.contributor.authorscopusid | 15829708200 | |
dc.contributor.authorscopusid | 7003855087 | |
dc.contributor.authorscopusid | 6507421079 | |
dc.contributor.authorscopusid | 24402677200 | |
dc.contributor.authorscopusid | 7202860969 | |
dc.contributor.authorscopusid | 6602879639 | |
dc.contributor.authorscopusid | 7004374085 | |
dc.description.lastpage | 589 | |
dc.description.firstpage | 585 | |
dc.relation.volume | 122 | |
dc.type2 | Artículo | es |
dc.contributor.daisngid | 465624 | |
dc.contributor.daisngid | 802813 | |
dc.contributor.daisngid | 1285881 | |
dc.contributor.daisngid | 2045042 | |
dc.contributor.daisngid | 4381521 | |
dc.contributor.daisngid | 1143821 | |
dc.contributor.daisngid | 591076 | |
dc.contributor.wosstandard | WOS:Henriquez-Hernandez, LA | |
dc.contributor.wosstandard | WOS:Lloret, M | |
dc.contributor.wosstandard | WOS:Pinar, B | |
dc.contributor.wosstandard | WOS:Bordon, E | |
dc.contributor.wosstandard | WOS:Rey, A | |
dc.contributor.wosstandard | WOS:Lubrano, A | |
dc.contributor.wosstandard | WOS:Lara, PC | |
dc.date.coverdate | Septiembre 2011 | |
dc.identifier.ulpgc | Sí | es |
dc.description.sjr | 2,06 | |
dc.description.jcr | 3,888 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q1 | |
dc.description.scie | SCIE | |
item.fulltext | Sin texto completo | - |
item.grantfulltext | none | - |
crisitem.author.dept | GIR IUIBS: Medio Ambiente y Salud | - |
crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.dept | Departamento de Ciencias Clínicas | - |
crisitem.author.orcid | 0000-0003-3237-0316 | - |
crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.fullName | Henríquez Hernández, Luis Alberto | - |
crisitem.author.fullName | Bordón Rodríguez, Elisa de los Reyes | - |
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