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Journal of Central South University(Medical Sciences) ; (12): 1128-1136, 2016.
Artículo en Chino | WPRIM | ID: wpr-815121

RESUMEN

To investigate the effect of jianpi-jiedu (JPJD) prescription-contained serum on colorectal cancer SW48 cell proliferation and the underlying mechanisms.
 Methods: Crude extract from JPJD was made by water extract method and the main components of crude extract from JPJD were analyzed by ultra-performance liquid phase high resolution time of flight mass spectrometry (UPLC-Q-TOF/MS). The low, medium, and high-concentration of JPJD-contained serum were prepared by the serum pharmacological method. The effect of serum containing JPJD on SW48 cell proliferation was determined by MTT assay. The cell cycle was detected by flow cytometric method. The protein levels of mammalian target of rapamycin (mTOR), phospho-mTOR, P-P53, and -P21, and the mRNA level of mTOR were examined by Western blot and RT-PCR, respectively.
 Results: Seven compounds including calycosin-7-glucoside, astragaloside, ginsenoside-Re, ginsenoside-Rb1, glycyrrhizinic acid, apigenin, atractylenolide-II were identified. MTT assays demonstrated that the SW48 cell proliferation was inhibited by medium and high concentration of JPJD-contained serum and the percentages of cells at G1 phase in SW48 cell cultured in the medium and high concentration of JPJD serum group were significantly higher than those in the control group (P<0.05). Meanwhile, the levels of mTOR mRNA and phospho-mTOR protein in the medium and high concentration of JPJD serum groups were substantially lower than those in the control group (P<0.05). Conversely, the expressions of phospho-P53 and P21 protein were significantly increased in the medium and high concentration of JPJD serum group compared with those in the control group.
 Conclusion: JPJD prescription-contained serum can inhibit SW48 cell proliferation, which may be related to mTOR-P53-P21 signaling pathways.


Asunto(s)
Animales , Humanos , Apigenina , Western Blotting , Ciclo Celular , División Celular , Proliferación Celular , Genética , Neoplasias Colorrectales , Inhibidor p21 de las Quinasas Dependientes de la Ciclina , Medicamentos Herbarios Chinos , Farmacología , Citometría de Flujo , Ginsenósidos , Ácido Glicirrínico , Lactonas , Fosforilación , Genética , ARN Mensajero , Saponinas , Sesquiterpenos , Transducción de Señal , Serina-Treonina Quinasas TOR , Triterpenos , Proteína p53 Supresora de Tumor
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