In vitro determination of radiation sensitivity parameters for DU-145 prostate cancer cells

被引:11
|
作者
Wang, Jian Z. [1 ]
Rhee, Juong G. [2 ]
Shi, Peipei
Stewart, Robert D. [3 ]
Li, X. Allen [4 ]
机构
[1] Ohio State Univ, Solove Res Inst, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Radiat Oncol, Baltimore, MD USA
[3] Purdue Univ, Sch Hlth Sci, W Lafayette, IN 47907 USA
[4] Med Coll Wisconsin, Dept Radiat Oncol, Milwaukee, WI 53226 USA
关键词
prostrate cancer; in vitro measurement; linear-quadratic model; repair half-time;
D O I
10.1080/09553000802061285
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: The prolonged delivery times associated with intensity modulated radiation therapy (IMRT) may reduce treatment effectiveness of radiation therapy for cancers with short repair half-times. In this study, invitro radiation experiments with DU-145 prostate cancer cells were designed to quantify the half-time of sublethal damage repair. Method and materials: A series of single-fraction and split-dose clonogenic survival experiments were performed and analyzed using the linear-quadratic (LQ) survival model with mono-/two-component exponential and reciprocal-time repair kinetic models. Results: Our data indicate that DU-145 cells are very radiosensitive (=0.44 Gy-1, standard CI: 0.41-0.49 Gy-1) and are relatively insensitive to dose fractionation (/=16 Gy, standard CI: 12-34 Gy). The estimated repair half-time is 23min (standard CI: 10-97min) with some evidence that a small portion of the sublethal damage is repaired more slowly. Conclusion: The reported radiosensitivity parameters ( and /) are larger than those derived from other invitro experiments and clinical data. In contrast, the half-time for sublethal damage repair (23min) is close to the one derived from clinical data (16min). For such short repair half-times, the effectiveness of IMRT treatments may be substantially improved by decreasing the fraction delivery time.
引用
收藏
页码:515 / 522
页数:8
相关论文
共 50 条
  • [41] Thrombin stimulates expression of the receptor for urokinase-type plasminogen activator in DU-145 prostate cancer cells
    Yoshida, E
    Verrusio, EN
    Mihara, H
    Oh, DY
    Kwaan, HC
    FIBRINOLYSIS & PROTEOLYSIS, 1997, 11 (03): : 147 - 154
  • [42] Anti-Proliferative Activity of Poloxamer Cobalt Ferrite Nanoparticles against Human Prostate Cancer (DU-145) Cells: In-Vitro Study
    Oroskhani, Nazanin
    Amini, Seyed Mohammad
    Shirvalilou, Sakine
    Khodaie, Mehdi
    Mahdavi, Seyed Rabi
    IET NANOBIOTECHNOLOGY, 2024, 2024 (01)
  • [43] NEK6 Regulates Redox Balance and DNA Damage Response in DU-145 Prostate Cancer Cells
    Pavan, Isadora Carolina Betim
    Basei, Fernanda Luisa
    Severino, Matheus Brandemarte
    Rosa e Silva, Ivan
    Issayama, Luidy Kazuo
    Mancini, Mariana Camargo Silva
    Gois, Mariana Marcela
    da Silva, Luiz Guilherme Salvino
    Bezerra, Rosangela Maria Neves
    Simabuco, Fernando Moreira
    Kobarg, Jorg
    CELLS, 2023, 12 (02)
  • [44] Expression of the receptor for urokinase-type plasminogen activator is increased by thrombin in DU-145 prostate cancer cells
    Yoshida, E
    Kwaan, HC
    Verrusio, EN
    BLOOD, 1995, 86 (10) : 2979 - 2979
  • [45] Effect of fatty acids on estradiol and testosterone binding to whole DU-145 prostate cells
    Prinsloo, SE
    van Aswegen, CH
    PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2002, 66 (04): : 419 - 425
  • [46] Estrogen receptors regulate galectin-3 in androgen-independent DU-145 prostate cancer cells
    Souza, Deborah S.
    Macheroni, Carla
    Vicente, Carolina M.
    Cavalheiro, Renan P.
    Campo, Vanessa L.
    Porto, Catarina S.
    ONCOLOGY REPORTS, 2023, 49 (05)
  • [47] Inhibition of Proliferation of Prostate Cancer Cell Line DU-145 in vitro and in vivo Using Salvia miltiorrhiza Bunge.
    Woong Jin Bae
    Jin Bong Choi
    Kang Sup Kim
    U. Syn Ha
    Sung Hoo Hong
    Ji Youl Lee
    Tae-Kon Hwang
    Sung Yeoun Hwang
    Zhi-ping Wang
    Sae Woong Kim
    Chinese Journal of Integrative Medicine, 2020, 26 : 533 - 538
  • [48] In vitro cytotoxic activity of anthrapyrazole analogues in human prostate DU-145 and testicular NTERA-2 carcinoma cells
    Cuevas, Maria E.
    Seilheimer, Kurt
    ONCOLOGY REPORTS, 2008, 20 (01) : 239 - 244
  • [49] IN-VITRO INVASIVENESS OF DU-145 PROSTATE CARCINOMA-CELLS IS MODULATED BY EGF RECEPTOR-MEDIATED SIGNALS
    XIE, H
    WANG, MH
    SINGH, RK
    SIEGAL, GP
    WELLS, A
    FASEB JOURNAL, 1995, 9 (03): : 137 - 137
  • [50] Pro-apoptotic substances induce ultrastructural modifications in "in vitro"-treated DU-145 human prostate carcinoma cells
    Rasa, DG
    Sinatra, F
    Chionna, A
    Dini, L
    PROCEEDINGS OF THE 5TH MULTINATIONAL CONGRESS ON ELECTRON MICROSCOPY, 2001, : 243 - 244