PRODUCCIÓN CIENTÍFICA (PCPLC)

A R T Í C U L O S

> Sánchez-Sánchez, L., Alvarado-Sansininea, J.J., Escobar, M.L., López-Muñoz, H., Hernández-Vázquez, J.M.V., Monsalvo-Montiel, I., Demare, P., Regla, I., Weiss-Steider, B.
Evaluation of the antitumour activity of Rinvanil and Phenylacetylrinvanil on the cervical cancer tumour cell lines HeLa, CaSKi and ViBo (2015) European Journal of Pharmacology (IF 2.5; Q2), 758, pp. 129-136. ISSN: 0014-2999, eISSN: 1879-0712

> Rojas-Oviedo, I; Camacho-Camacho, C; Sanchez-Sanchez, L; Cardenas, J; Lopez-Munoz, H; Eugenio-Robledo, H; Velazquez, I; Toscano, RA. Synthesis and characterization of tributyltin derivatives from 4-oxo-4-(arylamino)butanoic acids and their in vitro biological activity against cervical cancer cell lines. APPLIED ORGANOMETALLIC CHEMISTRY (IF 2.2 Q2 ). 28 (12): 884-891. ISSN: 0268-2605, eISSN: 1099-0739

> Sanchez-Sanchez, L; Escobar, ML; Sandoval-Ramirez, J; Lopez-Munoz, H; Fernandez-Herrera, MA; Hernandez-Vazquez, JMV; Hilario-Martinez, C; Zenteno, E. Apoptotic and autophagic cell death induced by glucolaxogenin in cervical cancer cells. APOPTOSIS (IF 3.6; Q2): 20(12): 1623-1635. ISSN: 1360-8185, eISSN: 1573-675X

> Sánchez-Sánchez L, Fernández-Herrera M, Sandoval-Ramírez J, López-Muñoz H, Escobar-Sánchez M. Probing the selective antitumor activity of 22-oxo-26-selenocyanocholestane derivatives. European Journal of Medicinal Chemistry. 2014;74:451-60.

> Sánchez-Sánchez L, López-Muñoz H, Escobar-Sánchez M, López-Marure R, Lascurain-Ledesma R, Zenteno-Galindo E, et al. Cervical cancer cells induce apoptosis in TCD4+ lymphocytes through the secretion of TGF-b. Arch Gynecol Obstet. 2013;287:755-63.

> Sánchez-Sánchez L, Fernández-Herrera M, López-Muñoz H, Hernández-Vázquez J, Escobar-Sánchez M, Pinto M, et al. Synthesis and selective anticancer activity of steroidal glycoconjugates. European Journal of Medicinal Chemistry. 2012;54:721-7.

 
 
 
> Sánchez-Sánchez L, López-Muñoz H, Fernández-Herrera M, Hernández-Vázquez J, López-Dávila M, Mohan S, et al. Synthesis of the cholestane glycoside (25R)-3β,16β-diacetoxy-22-oxocholest-5-en-26-yl β-D-glucopyranoside and its anticancer properties on cervicouterine cell lines. European Journal of Medicinal Chemistry. 2011;46:3877-86.

> Sánchez-Sánchez L, Escobar M, Echeverría O, Méndez M, Pedernera-Astegiano E, Vázquez-Nin G. Analysis of different cell death processes of prepubertal rat oocytes in vitro. Apoptosis. 2010;15:511-26.

> Sánchez-Sánchez L, Fernández-Herrera M, Mohan S, López-Muñoz H, Hernández-Vázquez J, Pérez-Cervantes E, et al. Synthesis of the steroidal glycoside (25R)-3b,16b-diacetoxy-12, 22-dioxo-5a-cholestan-26-yl b-D-glucopyranoside and its anti-cancer properties on cervicouterine HeLa, CaSki, and ViBo cells. European Journal of Medicinal Chemistry. 2010;45:4827-37.

> Sánchez-Sánchez L, Hernández-Herrera M, López-Muñoz H, Hernández-Vázquez J, López-Dávila M, Escobar-Sánchez M, et al. Synthesis of 26-hydroxy-22-oxocholestanic frameworks from diosgenin and hecogenin and their in vitro antiproliferative and apoptotic activity on human cervical cancer CaSki cells. Bioorganic & Medicinal Chemistry. 2010;18:2474-84.

> Sánchez-Sánchez L, Fernández-Herrera M, Sandoval-Ramírez J, López-Muñoz H. Formation of the steroidal 3b-hydroxy-6-oxo-moiety. Synthesis and cytototoxicity of glucolaxogenin. Arkivoc. 2009;XIII:170-84.