Immunohistochemical detection of p53 protein accumulation in head and neck cancer: Correlation with p53 gene alterations

1999 ◽  
Vol 30 (10) ◽  
pp. 1221-1225 ◽  
Author(s):  
David Taylor ◽  
Wayne M Koch ◽  
Marianna Zahurak ◽  
Keerti Shah ◽  
David Sidransky ◽  
...  
2015 ◽  
Vol 129 (4) ◽  
pp. 314-320 ◽  
Author(s):  
J P Hughes ◽  
G Alusi ◽  
Y Wang

AbstractBackground:Viral gene therapy is a promising new treatment modality for head and neck cancer. This paper provides the reader with a review of the relevant literature in this field.Results:There are government licensed viral gene therapy products currently in use for head and neck cancer, utilised in conjunction with established treatment modalities. The viruses target tumour-associated genes, with the first licensed virus replacing p53 gene function, which is frequently lost in tumourigenesis. Oncolytic viruses selectively destroy cancer cells through viral replication and can be armed with therapeutic transgenes.Conclusion:Despite considerable advances in this field over the last 40 years, further research is needed to improve the overall efficacy of the viruses and allow their widespread utilisation in the management of head and neck cancer.


1999 ◽  
Vol 10 (18) ◽  
pp. 2941-2952 ◽  
Author(s):  
Liang Xu ◽  
Kathleen F. Pirollo ◽  
Wen-Hua Tang ◽  
Antonina Rait ◽  
Esther H. Chang

Author(s):  
Ralf Erber ◽  
Wolfgang Klein ◽  
Thomas Andl ◽  
Christel Enders ◽  
Antonio I. Born ◽  
...  

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. e16011-e16011 ◽  
Author(s):  
Jihong Shu

e16011 Background: In head and neck cancer, p53 mutations are present in up 60% of head and neck cancers. Studies indicated p53 gene could increase both radio- and chemo-sensitivities. In this study, we investigate the effectiveness of recombinant adenoviral human p53 gene (rAd-p53) combined with chemoradiotherapy in treatment of advanced unresectable head and neck cancer. Methods: From May 2008 to Dec. 2011, 48 patients with an advanced unresectable head and neck cancer, 29 males and 18 females with an average of 61.3 years old, were included this study. Those patients were treated with intratumoral injection of rAd-p53 at a dose 1-3 ×1012 viral particles (VP) , once every 3 days for 6 times. Chemotherapy regimen consisted of cisplatin 60 mg/m2 on d1 and 5-Fu 600 mg/m2 on d1-5, given intravenously every 3 weeks for 3 cycles. Radiation were given at a dose of 2Gy/f, five fractions a week for a total dose 50~70Gy. Patients were monitored for response, long-term efficacy and adverse events. Results: The median follow-up time was 21.2 months (6~39 months). Overall response rate was 91.7% (44/48), 47.9% (23/48) of complete responses and 43.8% (23/48) of partial responses. One-year overall survival was 79.2% and local progression-free survival was 70.8%. At the last follow-up, the overall survival was 72.9%. Forty-six patients experienced self-limited fever after administration of p53. Conclusions: rAd-p53 gene therapy as a component of comprehensive treatment for advanced unresectable head and neck cancer showed significant beneficial effects.


The Lancet ◽  
1992 ◽  
Vol 339 (8791) ◽  
pp. 502-503 ◽  
Author(s):  
J.K. Field ◽  
D.A. Spandidos ◽  
P.M. Stell

2008 ◽  
Vol 184 (8) ◽  
pp. 393-399 ◽  
Author(s):  
Matthias Kappler ◽  
Helge Taubert ◽  
Hans-Jürgen Holzhausen ◽  
Rolf Reddemann ◽  
Swetlana Rot ◽  
...  

Author(s):  
Hitoshi Kawamata ◽  
Fumie Omotehara ◽  
Koh-Ichi Nakashiro ◽  
Daisuke Uchida ◽  
Yasuhiro Shinagawa ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Maria J. Worsham ◽  
Mei Lu ◽  
Kang Mei Chen ◽  
Josena K. Stephen ◽  
Shaleta Havard ◽  
...  

Genetic events specific to the pathogenesis of malignancy can offer clues to the tumorigenesis process. The objective of this study was to identify gene alterations that differentiate tumor and nontumor lesions in squamous head and neck cancer (HNSCC). DNA from 220 primary HNSCC with concurrently present tumor and nontumor lesions from the same patient was interrogated for genomic alterations of loss or gain of copy. Conditional logistic regression dealt with tumor and non-tumor records within a patient. Of 113 genes, 53 had univariate effects (P<0.01), of which 16 genes remained in the multivariable model withP<0.01. The model had a C-index (ROC) of 0.93. Loss ofCDKN2Band gain ofBCL6, FGF3, andPTP4A3predicted tumor. Loss ofBAK1andCCND1and gain ofSTCHpredicted nontumor. This highly powered model assigned alterations in 16 genes specific for malignant versus nonmalignant lesions, supporting their contribution to the pathogenesis of HNSCC as well as their potential utility as relevant targets for further evaluation as markers of early detection and progression.


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