Combination of 2-methoxyestradiol (2ME) and cyclophosphamide (CP) inhibits tumour progression in S-180 mouse tumour model system

被引:1
|
作者
Mallick S. [1 ]
Chowdhury S. [1 ]
Banerjee A. [1 ]
Paul G. [2 ]
Banerjee S.N. [1 ]
机构
[1] Department of Zoology, Rammohan College, 102/1, Raja Rammohan Sarani, Kolkata
[2] Department of Physiology, University of Kalyani, Kalyani, Nadia
关键词
2- Methoxyestradiol (2ME); Cell proliferation rate; Cyclophosphamide (CP); Mitotic index;
D O I
10.1007/s13237-017-0204-9
中图分类号
学科分类号
摘要
2-Methoxyestradiol (2ME), an anti-neoplastic and anti-angiogenic agent, has been used in preclinical research for cancer treatment. Cyclophosphamide (CP), the anti-neoplastic and alkaloid drug, has long been used as a traditional chemotherapeutic drug against different human neoplastic diseases. Our earlier studies showed that 2ME inhibit angiogenesis and cell proliferation rate differently in vivo and in vitro tumour models. But little work has been done on the combination effect of 2ME and CP on tumour model system. Therefore, the present study has been oriented to evaluate the efficacy and safety of combination effect of 2ME and CP on Sarcoma-180 tumour model system. In the present paper, an attempt has also been taken to find out whether the combination effect of 2ME and CP is less toxic than the traditional chemotherapeutic drug-CP, considering S-180 tumour bearing mouse bone marrow and germ cell toxicity as parameters and chromosomal aberrations, metaphase index and sperm head abnormality as biological endpoints. The result of these studies showed significant regression in tumour growth with inhibition of viable cancer cell population and less toxicity in the somatic and germinal cell of tumour bearing mouse. © 2017, Archana Sharma Foundation of Calcutta.
引用
收藏
页码:147 / 153
页数:6
相关论文
共 18 条
  • [11] Siah2 regulates tumour progression and neo-angiogenesis in a mouse model of breast cancer
    Wong, C. S. F.
    House, C. M.
    Liu, M. C. P.
    Haviv, I.
    Bowtell, D. D. L.
    Moeller, A.
    EJC SUPPLEMENTS, 2010, 8 (05): : 110 - 111
  • [12] The effect of rhIGF-1 and insulin analogue AspB10 on mammary tumour growth and progression in a mouse model of type 2 diabetes
    Gallagher, E. J.
    Alikhani, N.
    Tobin-Hess, A.
    Cannata, D.
    Tennagels, N.
    Werner, U.
    LeRoith, D.
    DIABETOLOGIA, 2012, 55 : S289 - S289
  • [13] Treatment based on a combination of the CYP2B1/cyclophosphamide system and p53 delivery enhances tumour regression in human pancreatic cancer
    Mercadé, E
    Cascalló, M
    Carrió, M
    Calbó, J
    Gómez-Treviño, A
    Fillat, C
    Gómez-Foix, AM
    Mazo, A
    ANNALS OF ONCOLOGY, 2001, 12 (03) : 379 - 388
  • [14] Inhibition of tumour necrosis factor alpha in the R6/2 mouse model of Huntington's disease by etanercept treatment
    Pido-Lopez, Jeffrey
    Tanudjojo, Benedict
    Farag, Sahar
    Bondulich, Marie-Katrin
    Andre, Ralph
    Tabrizi, Sarah J.
    Bates, Gillian P.
    SCIENTIFIC REPORTS, 2019, 9 (1)
  • [15] Inhibition of tumour necrosis factor alpha in the R6/2 mouse model of Huntington’s disease by etanercept treatment
    Jeffrey Pido-Lopez
    Benedict Tanudjojo
    Sahar Farag
    Marie-Katrin Bondulich
    Ralph Andre
    Sarah J. Tabrizi
    Gillian P. Bates
    Scientific Reports, 9
  • [16] Combination treatment with Apo2L/TRAIL and radiation: Pre-clinical study on growth retardation and tumour healing under norm- and hypoxia in the naked mouse model
    Marini, P
    Welz, S
    Stasch, K
    Jendrossek, V
    Budach, W
    Belka, C
    STRAHLENTHERAPIE UND ONKOLOGIE, 2005, 181 : 96 - 96
  • [17] Gamma-linolenic acid inhibits both tumour cell cycle progression and angiogenesis in the orthotopic C6 glioma model through changes in VEGF, Flt1, ERK1/2, MMP2, cyclin D1, pRb, p53 and p27 protein expression
    Miyake, Juliano Andreoli
    Benadiba, Marcel
    Colquhoun, Alison
    LIPIDS IN HEALTH AND DISEASE, 2009, 8
  • [18] Gamma-linolenic acid inhibits both tumour cell cycle progression and angiogenesis in the orthotopic C6 glioma model through changes in VEGF, Flt1, ERK1/2, MMP2, cyclin D1, pRb, p53 and p27 protein expression
    Juliano Andreoli Miyake
    Marcel Benadiba
    Alison Colquhoun
    Lipids in Health and Disease, 8