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Radiation enhances cisplatin-sensitivity in human cervical squamous cancer cells in vitro
1Department of Obstetrics and Gynecology, Japan
2Department of Physiology, Wakayama Medical University, Wakayama, Japan
*Corresponding Author(s): T. Tanaka E-mail:
PURPOSE AND METHODS OF INVESTIGATION: Cisplatin (CDDP) is regularly used in concurrent chemoradiotherapy in patients with advanced cervical cancer although an effective protocol of chemoradiotherapy with CDDP has not yet been established. In search of a better chemoradiotherapy protocol, we investigated both CDDP effects on radiosensitivity and irradiation effects on CDDP-sensitivity using the radiosensitive human cervical squamous cell carcinoma cell line ME180.
Results: We found that CDDP did not affect cellular radiosensitivity, and that irradiation significantly enhanced CDDP-sensitivity. Moreover, all the four post-irradiation surviving subclones obtained from repetitively irradiated ME180 cells showed significantly higher CDDP sensitivities than those of the non-irradiated parent cells.
Conclusion: These results suggest that an effective protocol would involve the concurrent administration of CDDP with radiotherapy and further administration following completion of radiotherapy in order to achieve higher CDDP-sensitivities.
Cisplatin; Chemoradiotherapy; Cervical cancer; Squamous cell carcinoma; Radiosensitivity
T. Tanaka,K. Yukawa,N. Umesaki. Radiation enhances cisplatin-sensitivity in human cervical squamous cancer cells in vitro. European Journal of Gynaecological Oncology. 2005. 26(4);431-433.
[1] Whitney C.W., Sause W., Bundy B.N., Malfetano J.H., Hannigan E. V., Fowler W.C. Jr. et al.: "Randomized comparison of fluorouracil plus cisplayin versus hydroxurea as an adjunct to radiation therapy in stage 11B-IVA carcinoma of the cervix with negative para-aortic lymph nodes: a Gynecologic Oncology Group and Southeast Oncology Group Study". J. Clin. Oncol., 1999, 17, 1339.
[2] Morris M., Eifel P.J., Lu J., Grigsby P.W., Levenback C., Stevens R.E. et al.: "Pelvic radiation with concurrent chemotherapy compared with pelvic and para-aortic radiatiou for high-risk cervical cancer". New Eng. J. Med., 1999, 340, 1137.
[3] Rose P.G., Bundy B.N., Watkins E.B., T higpen J.T., Deppe G., Maiman M.A. et al.: "Concurrent cisplatin-based radiotherapy and chemotherapy for locally advanced cervical cancer". New Eng. J Med., 1999, 340, 1144.
[4] Keys H.M., Bundy B.N., Stehman F.B., Muderspach L.I., Chafe W.E., Suggs C.L. 3'' et al.: "Cisplatin, radiation, and adjuvant hysterectomy compared with radiation and adjuvant hysterectomy for bulky stage TB cervical carcinoma". New Eng. J. Med., 1999, 340, 1154.
[5] Peters W.A. 3'', Liu P.Y., Barrett R.J. 2"', Stock RJ, Monk B.J., Berek J.S. et al.: "Concurrent chemotherapy and pelvic radiation therapy compared with pelvic radiation therapy alone as adjuvant therapy after radical surgery in high-risk early-stage cancer of the cervix". J. Clin. Oncol., 2000, 18, 1606.
[6] Pearcey R., Brundage M., Drouin P., Jeffrey J., Johnston D., Lukka H. et al.: "Phase III trial comparing radical radiotherapy with and without cisplatin chemotherapy in patients with advanced squamous cell cancer of the cervix". J. Clin. Oncol., 2002, 20, 966.
[7] Tabata T., Takeshima N., Nishida H., Hirai Y., Hasumi K.: "A randomized study of primary bleomycin, vincristine, mitomycin and cisplatin (BOMP) chemotherapy followed by radiotherapy versus radiotherapy alone in stage IIIB and IVA squamous cell carcinoma of the cervix". Anticancer Res., 2003, 23, 2885.
[8] Lancillotti F., Giandomenico V., Affabris E., Fiorucci G., Romeo G., Rossi G.B.: "Interferon alpha-2b and retinoic acid combined treatment affects proliferation and gene expression of human cervical carcinoma cells". Cancer Res., 1995, 55, 3158.
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