Expression and heterodimer-binding activity of Ku70 and Ku80 in human non-melanoma skin cancer
Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. Aim: To investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas. Methods: Levels of Ku70 and Ku80 proteins were det...
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Published in: | Journal of clinical pathology Vol. 59; no. 11; pp. 1181 - 1185 |
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Abstract | Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. Aim: To investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas. Methods: Levels of Ku70 and Ku80 proteins were determined by immunohistochemical analysis and Ku70–Ku80 heterodimer-binding activity by electrophoretic mobility shift assay. Matched pathological normal margins and skin from healthy people were used as controls. Results: A significant increase in Ku70 and Ku80 protein levels was found for both tumour types as compared with normal skin (p<0.001). Squamous cell carcinoma showed increased immunostaining as compared with basal cell tumours (p<0.02). A direct correlation was found between Ku70 and Ku80 protein levels and expression of the proliferation markers Ki-67/MIB-1 (p<0.02 and p<0.002, respectively) in basal cell carcinoma. DNA binding activity was increased in basal cell carcinoma samples as compared with matched skin histopathologically negative for cancer (p<0.006). In squamous cell carcinomas, however, the difference was significant only with normal skin (p<0.02) and not with matched pathologically normal margins. Conclusions: Overall, an up regulation of the Ku70 and Ku80 protein levels seems to correlate only with tumour proliferation rate. As non-homologous end joining is an error-prone mechanism, its up regulation may ultimately increase genomic instability, contributing to tumour progression. |
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AbstractList | Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. Aim: To investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas. Methods: Levels of Ku70 and Ku80 proteins were determined by immunohistochemical analysis and Ku70-Ku80 heterodimer-binding activity by electrophoretic mobility shift assay. Matched pathological normal margins and skin from healthy people were used as controls. Results: A significant increase in Ku70 and Ku80 protein levels was found for both tumour types as compared with normal skin (p<0.001). Squamous cell carcinoma showed increased immunostaining as compared with basal cell tumours (p<0.02). A direct correlation was found between Ku70 and Ku80 protein levels and expression of the proliferation markers Ki-67/MIB-1 (p<0.02 and p<0.002, respectively) in basal cell carcinoma. DNA binding activity was increased in basal cell carcinoma samples as compared with matched skin histopathologically negative for cancer (p<0.006). In squamous cell carcinomas, however, the difference was significant only with normal skin (p<0.02) and not with matched pathologically normal margins. Conclusions: Overall, an up regulation of the Ku70 and Ku80 protein levels seems to correlate only with tumour proliferation rate. As non-homologous end joining is an error-prone mechanism, its up regulation may ultimately increase genomic instability, contributing to tumour progression. Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. To investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas. Levels of Ku70 and Ku80 proteins were determined by immunohistochemical analysis and Ku70-Ku80 heterodimer-binding activity by electrophoretic mobility shift assay. Matched pathological normal margins and skin from healthy people were used as controls. A significant increase in Ku70 and Ku80 protein levels was found for both tumour types as compared with normal skin (p<0.001). Squamous cell carcinoma showed increased immunostaining as compared with basal cell tumours (p<0.02). A direct correlation was found between Ku70 and Ku80 protein levels and expression of the proliferation markers Ki-67/MIB-1 (p<0.02 and p<0.002, respectively) in basal cell carcinoma. DNA binding activity was increased in basal cell carcinoma samples as compared with matched skin histopathologically negative for cancer (p<0.006). In squamous cell carcinomas, however, the difference was significant only with normal skin (p<0.02) and not with matched pathologically normal margins. Overall, an up regulation of the Ku70 and Ku80 protein levels seems to correlate only with tumour proliferation rate. As non-homologous end joining is an error-prone mechanism, its up regulation may ultimately increase genomic instability, contributing to tumour progression. Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. Aim: To investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas. Methods: Levels of Ku70 and Ku80 proteins were determined by immunohistochemical analysis and Ku70–Ku80 heterodimer-binding activity by electrophoretic mobility shift assay. Matched pathological normal margins and skin from healthy people were used as controls. Results: A significant increase in Ku70 and Ku80 protein levels was found for both tumour types as compared with normal skin (p<0.001). Squamous cell carcinoma showed increased immunostaining as compared with basal cell tumours (p<0.02). A direct correlation was found between Ku70 and Ku80 protein levels and expression of the proliferation markers Ki-67/MIB-1 (p<0.02 and p<0.002, respectively) in basal cell carcinoma. DNA binding activity was increased in basal cell carcinoma samples as compared with matched skin histopathologically negative for cancer (p<0.006). In squamous cell carcinomas, however, the difference was significant only with normal skin (p<0.02) and not with matched pathologically normal margins. Conclusions: Overall, an up regulation of the Ku70 and Ku80 protein levels seems to correlate only with tumour proliferation rate. As non-homologous end joining is an error-prone mechanism, its up regulation may ultimately increase genomic instability, contributing to tumour progression. BACKGROUNDExperimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks.AIMTo investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas.METHODSLevels of Ku70 and Ku80 proteins were determined by immunohistochemical analysis and Ku70-Ku80 heterodimer-binding activity by electrophoretic mobility shift assay. Matched pathological normal margins and skin from healthy people were used as controls.RESULTSA significant increase in Ku70 and Ku80 protein levels was found for both tumour types as compared with normal skin (p<0.001). Squamous cell carcinoma showed increased immunostaining as compared with basal cell tumours (p<0.02). A direct correlation was found between Ku70 and Ku80 protein levels and expression of the proliferation markers Ki-67/MIB-1 (p<0.02 and p<0.002, respectively) in basal cell carcinoma. DNA binding activity was increased in basal cell carcinoma samples as compared with matched skin histopathologically negative for cancer (p<0.006). In squamous cell carcinomas, however, the difference was significant only with normal skin (p<0.02) and not with matched pathologically normal margins.CONCLUSIONSOverall, an up regulation of the Ku70 and Ku80 protein levels seems to correlate only with tumour proliferation rate. As non-homologous end joining is an error-prone mechanism, its up regulation may ultimately increase genomic instability, contributing to tumour progression. |
Author | Signori, E Delfino, M Rinaldi, M Persichetti, P Perrone, G Parrella, P Rabitti, C Fabbrocini, G Marangi, G F Prencipe, M Fazio, V M Gallo, A P Delfino, S Mazzarelli, P |
AuthorAffiliation | G Perrone , C Rabitti , Laboratory of Hystopathology, Campus Bio‐Medico University, Rome, Italy P Mazzarelli , E Signori , V M Fazio , CIR, Section for Molecular Medicine and Biotechnology, Campus Bio‐Medico University, Rome, Italy G F Marangi , S Delfino , P Persichetti , Division of Plastic and Reconstructive Surgery, Campus Bio‐Medico University, Rome, Italy E Signori , M Rinaldi , CNR INMM, Laboratory of Gene Medicine, Area of Rome “Tar Vergata”, Rome, Italy M Delfino , G Fabbrocini , Department of Dermatology, University Federico II, Naples, Italy P Parrella , M Prencipe , A P Gallo , V M Fazio , Oncology Research Laboratory, IRCCS Hospital “Casa Sollievo della Sofferenza”, San Giovanni Rotondo (FG), Italy |
AuthorAffiliation_xml | – name: P Mazzarelli , E Signori , V M Fazio , CIR, Section for Molecular Medicine and Biotechnology, Campus Bio‐Medico University, Rome, Italy – name: P Parrella , M Prencipe , A P Gallo , V M Fazio , Oncology Research Laboratory, IRCCS Hospital “Casa Sollievo della Sofferenza”, San Giovanni Rotondo (FG), Italy – name: G Perrone , C Rabitti , Laboratory of Hystopathology, Campus Bio‐Medico University, Rome, Italy – name: E Signori , M Rinaldi , CNR INMM, Laboratory of Gene Medicine, Area of Rome “Tar Vergata”, Rome, Italy – name: M Delfino , G Fabbrocini , Department of Dermatology, University Federico II, Naples, Italy – name: G F Marangi , S Delfino , P Persichetti , Division of Plastic and Reconstructive Surgery, Campus Bio‐Medico University, Rome, Italy |
Author_xml | – sequence: 1 givenname: P surname: Parrella fullname: Parrella, P organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 2 givenname: P surname: Mazzarelli fullname: Mazzarelli, P organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 3 givenname: E surname: Signori fullname: Signori, E organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 4 givenname: G surname: Perrone fullname: Perrone, G organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 5 givenname: G F surname: Marangi fullname: Marangi, G F organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 6 givenname: C surname: Rabitti fullname: Rabitti, C organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 7 givenname: M surname: Delfino fullname: Delfino, M organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 8 givenname: M surname: Prencipe fullname: Prencipe, M organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 9 givenname: A P surname: Gallo fullname: Gallo, A P organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 10 givenname: M surname: Rinaldi fullname: Rinaldi, M organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 11 givenname: G surname: Fabbrocini fullname: Fabbrocini, G organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 12 givenname: S surname: Delfino fullname: Delfino, S organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 13 givenname: P surname: Persichetti fullname: Persichetti, P organization: Department of Dermatology, University Federico II, Naples, Italy – sequence: 14 givenname: V M surname: Fazio fullname: Fazio, V M organization: Department of Dermatology, University Federico II, Naples, Italy |
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Keywords | Human Binding Skin disease Anatomic pathology Malignant melanoma Malignant tumor Heterodimer Biological activity Skin cancer |
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Snippet | Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. Aim: To investigate the... Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. To investigate the contribution of the... Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks. Aim: To investigate the... BACKGROUNDExperimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks.AIMTo investigate the contribution of... |
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SubjectTerms | Antigens, Nuclear - metabolism basal cell carcinoma BCC Biological and medical sciences Biomarkers, Tumor - metabolism Carcinoma, Basal Cell - metabolism Carcinoma, Basal Cell - pathology Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - pathology Cell Proliferation Dermatology Disease Progression DNA-Binding Proteins - metabolism double-strand break DSB Electrophoretic Mobility Shift Assay EMSA Humans IHC immunohistochemical Investigative techniques, diagnostic techniques (general aspects) Ki-67 Antigen - metabolism Ku Autoantigen Medical sciences Neoplasm Proteins - metabolism NHEJ NMSC non-homologous end joining non-melanoma skin cancer Original Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques SCC Skin Neoplasms - metabolism Skin Neoplasms - pathology squamous cell carcinoma TBS TRIS-buffered saline Tumors of the skin and soft tissue. Premalignant lesions Up-Regulation |
Title | Expression and heterodimer-binding activity of Ku70 and Ku80 in human non-melanoma skin cancer |
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