مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

259
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

137
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

HUMAN PAPILLOMAVIRUS INFECTION, P53 OVER EXPRESSION AND HISTOPATHOLOGIC CHARACTERISTICS IN COLORECTAL CANCER

Pages

  126-133

Abstract

 Background: There is evidence of a possible etiological role of human papillomaviruses (HPVs) in the development of COLORECTAL CANCER. Loss of P53 tumor suppressor gene function has been found in many malignancies and it can occur in a variety of ways, including gene mutation and interaction with the E6 protein of oncogenic HPVs. The objective of this study was to determine the prevalence of HPV infection and P53 over expression in COLORECTAL CANCER (CRC) tissue samples and its association with tumor HISTOPATHOLOGIC CHARACTERISTICS. Materials and Methods: 60 tissue sections from patients with CRC were investigated by immunocytochemistry techniques for aberrant expression of P53 using the streptavidin-biotin-peroxidase method with monoclonal antibodies. The HPV status was also analyzed using type-specific primers for HPV16/18by polymerase chain reaction (PCR). Results: Overall, 21 (35%) of 60 patients were found positive for HPV DNA; HPV 18was detected in 19 (32%) and HPV 16 in 11 (18%) of 60 samples. An abnormal expression of tumor-suppressor protein P53 was observed in 29 (48%) samples. P53 over expression was observed in 15 (71%) of 21 HPV-positive and in 14 (36%) of 39 HPV-negative patients (p=0.009). Similar significant difference was found in P53 over expression in HPV18-positive patients (p=0.007) but not in those positive for HPV 16 (p=0.261). HPV DNA presentation was not significantly associated with HISTOPATHOLOGIC CHARACTERISTICS including tumor stage (p=0.509), grade (p=0.668), peri-neural invasion (p=0.265) and Iympho-vascular invasion (p=0.275). Conclusions: P53 inactivation caused by HPV infection may play a role in the pathogenesis of COLORECTAL CANCER. There is no association between HPV infection and HISTOPATHOLOGIC CHARACTERISTICS.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    MOTLAGH, A., AZADEH, P., HASHEMI, M., SHAFAGHI, B., NOURI NAYER, B., MOULAEI, M., SHEYBANI, KH.M., FAZL ALIZADEH, A., FOUDAZI, M., VELAEI, N., GHADERI, F., DAVAEI, M., & ZALI, MOHAMMAD REZA. (2007). HUMAN PAPILLOMAVIRUS INFECTION, P53 OVER EXPRESSION AND HISTOPATHOLOGIC CHARACTERISTICS IN COLORECTAL CANCER. GOVARESH JOURNAL, 12(2), 126-133. SID. https://sid.ir/paper/545417/en

    Vancouver: Copy

    MOTLAGH A., AZADEH P., HASHEMI M., SHAFAGHI B., NOURI NAYER B., MOULAEI M., SHEYBANI KH.M., FAZL ALIZADEH A., FOUDAZI M., VELAEI N., GHADERI F., DAVAEI M., ZALI MOHAMMAD REZA. HUMAN PAPILLOMAVIRUS INFECTION, P53 OVER EXPRESSION AND HISTOPATHOLOGIC CHARACTERISTICS IN COLORECTAL CANCER. GOVARESH JOURNAL[Internet]. 2007;12(2):126-133. Available from: https://sid.ir/paper/545417/en

    IEEE: Copy

    A. MOTLAGH, P. AZADEH, M. HASHEMI, B. SHAFAGHI, B. NOURI NAYER, M. MOULAEI, KH.M. SHEYBANI, A. FAZL ALIZADEH, M. FOUDAZI, N. VELAEI, F. GHADERI, M. DAVAEI, and MOHAMMAD REZA ZALI, “HUMAN PAPILLOMAVIRUS INFECTION, P53 OVER EXPRESSION AND HISTOPATHOLOGIC CHARACTERISTICS IN COLORECTAL CANCER,” GOVARESH JOURNAL, vol. 12, no. 2, pp. 126–133, 2007, [Online]. Available: https://sid.ir/paper/545417/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button