scholarly journals Progesterone Induces the Growth and Infiltration of Human Astrocytoma Cells Implanted in the Cerebral Cortex of the Rat

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Liliana Germán-Castelán ◽  
Joaquín Manjarrez-Marmolejo ◽  
Aliesha González-Arenas ◽  
María Genoveva González-Morán ◽  
Ignacio Camacho-Arroyo

Progesterone (P4) promotes cell proliferation in several types of cancer, including brain tumors such as astrocytomas, the most common and aggressive primary intracerebral neoplasm in humans. In this work, we studied the effects of P4and its intracellular receptor antagonist, RU486, on growth and infiltration of U373 cells derived from a human astrocytoma grade III, implanted in the motor cortex of adult male rats, using two treatment schemes. In the first one, fifteen days after cells implantation, rats were daily subcutaneously treated with vehicle (propylene glycol, 160 μL), P4(1 mg), RU486 (5 mg), or P4+ RU486 (1 mg and 5 mg, resp.) for 21 days. In the second one, treatments started 8 weeks after cells implantation and lasted for 14 days. In both schemes we found that P4significantly increased the tumor area as compared with the rest of the treatments, whereas RU486 blocked P4effects. All rats treated with P4showed tumor infiltration, while 28.6% and 42.9% of the animals treated with RU486 and P4+ RU486, respectively, presented it. Our data suggest that P4promotes growth and migration of human astrocytoma cells implanted in the motor cortex of the rat through the interaction with its intracellular receptor.

2010 ◽  
Vol 2010 ◽  
pp. 1-10 ◽  
Author(s):  
Abdelkader Hamadi ◽  
Therese B. Deramaudt ◽  
Kenneth Takeda ◽  
Philippe Rondé

Cell adhesion and migration are key determinants in tumor metastasis. Adherence of tumor cell to the extracellular matrix is mediated via integrin containing focal adhesions (FAs). Binding of integrins to ECM triggers phosphorylation of two major components of FAs, focal adhesion kinase (FAK) and Src, activating downstream signaling pathway which leads to FA disassembly and cell migration. In this paper, we analyze how phosphorylation of FAK regulates its trafficking at FAs in living human astrocytoma cells. Upon pervanadate-induced FAK phosphorylation, phosphorylated FAK appeared highly expressed at newly formed membrane ruffles. This effect was abolished in presence of the specific Src inhibitor PP2. Our findings demonstrate that upon phosphorylation, FAK delocalizes from FAs to membrane ruffles.


Glia ◽  
1995 ◽  
Vol 13 (1) ◽  
pp. 64-74 ◽  
Author(s):  
Alf Giese ◽  
Monique D. Rief ◽  
Nhan L. Tran ◽  
Michael E. Berens

Steroids ◽  
2016 ◽  
Vol 105 ◽  
pp. 19-25 ◽  
Author(s):  
Ana Gabriela Piña-Medina ◽  
Valeria Hansberg-Pastor ◽  
Aliesha González-Arenas ◽  
Marco Cerbón ◽  
Ignacio Camacho-Arroyo

1991 ◽  
Vol 568 (1-2) ◽  
pp. 92-100 ◽  
Author(s):  
Jose L. Tomsig ◽  
Eric Gruenstein ◽  
Ruth V.W. Dimlich

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