Publications by authors named "Jian-Xiu Ma"

Article Synopsis
  • The study aimed to explore the DNA damage response (DDR) in mice undergoing premature ovarian failure (POF) induced by cyclophosphamide (CTX).
  • The results showed that CTX treatment led to decreased body and ovarian weights, irregular estrus cycles, and hormonal changes, indicating significant ovarian dysfunction in the POF model.
  • The findings suggest that CTX-induced POF in mice is linked to the activation of the DDR pathway involving ATM, P53, and P21, highlighting the potential mechanisms behind ovarian failure.
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Background: H2AX is phosphorylated (γH2AX) by members of the phosphatidylinositol 3-kinase (PI3K) family, including Ataxia telangiectasia-mutated (ATM), ATM- and Rad3-related (ATR) and DNA-PK in response to DNA damage. Our study shows that gossypol acetic acid (GAA) alone can induce γH2AX in Human mucoepidermoid carcinoma cell line (MEC-1) in vitro. Thus, we further examined the possible mechanisms of GAA to induce γH2AX in tumor cells.

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The present study was conducted to investigate the effects of gossypol acetic acid (GAA) on the proliferation of human mucoepidermoid carcinoma cell line MEC-1 in vitro and its possible molecular mechanisms of DNA double-strand breaks (DSB). MTT assay was performed to test the inhibition of proliferation of MEC-1 cells by GAA. DSB and γH2AX foci formation induced by GAA were detected by neutral comet assay and immunostaining.

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Objective: To observe the influence of matrine on airway inflammation and early airway remodeling in asthmatic mice.

Methods: Fifty BALB/c mice were randomly divided into 5 groups: a normal control group (A), an asthmatic group (B), a dexamethasone (DXM) group (C, 2 mg/kg), a high-dose matrine group (D, 50 mg/kg) and a low-dose matrine group (E, 25 mg/kg). The mice model of asthma in the B, C, D, and E groups was established by ovalbumin (OVA) intraperitoneal injections and aerosolization.

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