Effect of hexachlorobenzene (hcb) and protein x of the hepatitis b virus (hbv) on liver cell growth dysregulation
; Miret, Noelia ; Oubiña, Jose Raul
; Alvarez, Laura Fecha
2021
Editorial
Fundación Revista Medicina
Revista
Título del libro
Nombre del evento
LXVI Reunión Anual de La Sociedad Argentina de Investigación Clínica; LXIX Reunión Anual de La Sociedad Argentina de Inmunología; LIII Reunión Anual de La Asociación Argentina de Farmacología Experimental y XI Reunión Anual de La Asociación Argentina De Nanomedicinas
Fecha del evento
2021-11-17
Institución organizadora
Sociedad Argentina de Investigación Clínica
Sociedad Argentina de Inmunología
Asociación Argentina de Farmacología Experimental
Asociación Argentina de Nanomedicinas
Sociedad Argentina de Inmunología
Asociación Argentina de Farmacología Experimental
Asociación Argentina de Nanomedicinas
ISSN
1669-9106
eISSN
0025-7680
ISBN
Idioma
Inglés
Tipo del evento
Reunión
Clasificación temática
Palabras clave
Resumen
Chronic hepatitis B and exposure to persistent organic pollutants (POPs) can lead to cellular hepatocarcinoma (HCC), the most common liver tumor. HBV DNA encodes transactivator X (HBx). HCB is a COP promoter of hepatic preneoplastic foci. We have shown that HCB deregulates cell growth in rat liver and HepG2 cells, involving TGF-β1, a reversed effect with an Rβ1 inhibitor. Objectives: To analyze in vitro 2 models of HCC generation -associated to HCB or to the expression of HBx- and in vivo the hepatic and angiogenic promoter HCB effect in Balb/c nude mice inoculated with HepG2. M&M: the HCB effect on PCNA (Western blot)/TGF-β1 (RT-PCR) was studied in vitro in: 1.1) Huh-7: HCB at various doses (0.005, 0.05, 0.5 and 5 µM ) and times (15, 30, 60, 90 and 120 min); 1.2) Huh-7 transiently transfected with HBx; 2) HepG2.2.15 (with stable expression of HBV) and 3) EA-hy926 (endothelial). In 1.2, 2 and 3 5 µM HCB, 24h was used. Mice: HCB i.p. (0.3 and 3 mg/ kg), and were inoculated with HepG2. Were evaluated: a) PCNA, b) TGF-β1, c) No . of tumor areas, d) histology (H&E) and e) No . of vessels/mm2 . Results: In Huh-7, TGF-β1 increased (20%, p <0.05; 69% and 78%, p <0.01, with 0.05, 0.5 and 5 µM HCB, respectively) and PCNA (45% and 60%, p <0.01, with 0.5 and 5 µM HCB, respectively). In Huh-7 / HBx, PCNA and TGF-β1 increased 66% and 71% (p <0.01). In Huh-7 / HBx and 5 µM HCB, PCNA increased 120% (p <0.001). In HepG2.2.15 PCNA was overexpressed 76% (p <0.001). In EA-hy926, PCNA (29%, p <0.05) and TGF-β1 (43%, p <0.01) increased. In mice, PCNA (39%; p <0.01), TGF-β1 (48%; p <0.01), preneoplastic areas (320%; p <0.001) and vascularization (35%; p <0.01). Conclusions: HCB promotes preneoplastic cell proliferation and angiogenesis in nude mice inoculated with HepG2, while HCB and HBx induce in vitro cell proliferation associated with the increase of TGF-β1 in the examined lines, a proliferative effect increased to that promoted by the HCB being able to participate in the induction of HCC.
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