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TAT-RasGAP 317-326 Enhances Radiosensitivity of Human Carcinoma Cell Lines In Vitro and In Vivo through Promotion of Delayed Mitotic Cell Death.
- Source :
-
Radiation research [Radiat Res] 2017 May; Vol. 187 (5), pp. 562-569. Date of Electronic Publication: 2017 Mar 21. - Publication Year :
- 2017
-
Abstract
- The synthetic peptide TAT-RasGAP <subscript>317-326</subscript> has been shown to potentiate the efficacy of anti-cancer drugs. In this study, we explored the action of TAT-RasGAP <subscript>317-326</subscript> when combined with radiation by investigating its radiosensitizing activity in vitro and in vivo. To investigate the modulation of intrinsic radiosensitivity induced by TAT-RasGAP <subscript>317-326</subscript> , clonogenic assays were performed using four human cancer cell lines, HCT116 p53 <superscript>+/+</superscript> (ATCC: CCL-247), HCT116 p53 <superscript>-/-</superscript> , PANC-1 (ATCC: CRL-1469) and HeLa (ATCC: CCL-2), as well as one nontumor cell line, HaCaT (CLS: 300493). Next, to investigate tumor growth delay after irradiation, HCT116 cell lines were selected and xenografted onto nude mice that were then treated with TAT-RasGAP <subscript>317-326</subscript> alone or in combination with radiation or cisplatin. Afterwards, cell cycle and death modulation were investigated by quantification of micronuclei and apoptosis-related protein array. TAT-RasGAP <subscript>317-326</subscript> radiosensitized all four human carcinoma cell lines tested but displayed no effect on normal cells. It also displayed no effect when administered as monotherapy. This radiosensitizing effect was confirmed in vivo in both p53-positive and p53-negative HCT116 xenografts. TAT-RasGAP <subscript>317-326</subscript> combined with radiation enhanced the number of cells in S phase and subsequently delayed cell death, but had almost no effect on major apoptosis-related proteins. TAT-RasGAP <subscript>317-326</subscript> is a radiosensitizing agent that acts on carcinoma cells and its radiosensitizing effect might be mediated, at least in part, by the enhancement of mitotic cell death.
- Subjects :
- Apoptosis drug effects
Cell Line, Tumor
Dose-Response Relationship, Drug
HCT116 Cells
HeLa Cells
Humans
Mitosis drug effects
Radiation-Sensitizing Agents administration & dosage
Radiotherapy Dosage
Treatment Outcome
Apoptosis radiation effects
GTPase-Activating Proteins administration & dosage
Mitosis radiation effects
Neoplasms, Experimental pathology
Neoplasms, Experimental radiotherapy
Peptide Fragments administration & dosage
Radiation Tolerance drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1938-5404
- Volume :
- 187
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Radiation research
- Publication Type :
- Academic Journal
- Accession number :
- 28323576
- Full Text :
- https://doi.org/10.1667/RR14509.1