Asiatic Acid Promotes p21WAF1/CIP1 Protein Stability in HepG2 Human Hepatoma Cells

نویسندگان

  • Jin-Yuan Chen
  • Qing-Wen Xu
  • Hong Xu
  • Zong-Hai Huang
چکیده

More than 60% of currently used anti-tumor drugs are natural origin or derived from natural compounds (Cragg et al., 2005). Plant-derived compounds are important source of these nature derived anti-tumor agents. Nearly 3000 plant species have been reported for the treatment of cancer (Altinbas et al., 2012; Boreddy et al., 2013). Some plant based anticancer agents have been allowed to enter the clinical trial, such as paclitaxel, vincristine, vinblastine, topotecan and irinotecan (Nobili et al., 2009). Asiatic acid, a pentacyclic triterpene found in the tropical medicinal plant Centella asiatica, has antioxidant, antiinflammatory and neuroprotective properties (Huang et al., 2012; Guo et al., 2013). Some studies have reported the anti-tumor effect of asiatic acid. For example, asiatic acid was reported to enhance apoptosis and cell cycle arrest by promoting the activity of extracellular signalregulated kinase and p38 mitogen-activated protein kinase pathways in human breast cancer cells (Hsu et al., 2005). By generation of ROS, asiatic acid could induce apoptosis in human melanoma cells (Park et al., 2005; Xu

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Posttranscriptional regulation of p21WAF1/CIP1 expression in human breast carcinoma cells.

p21WAF1/CIP1 plays a major role in the induction of G1 arrest following DNA damage. Although p21WAF1/CIP1 expression is regulated by the tumor suppressor p53, induction of p21WAF1/CIP1 expression through p53-independent pathways has been described in numerous cell types. In this report, we describe the mechanism by which the retinoid 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphthalene carboxylic ...

متن کامل

Acyclic retinoid activates retinoic acid receptor beta and induces transcriptional activation of p21(CIP1) in HepG2 human hepatoma cells.

Acyclic retinoid (ACR), a novel synthetic retinoid, has recently been demonstrated by us to inhibit the in vitro growth of human hepatoma cells, and this effect was associated with decreased expression of cell cycle-related molecules. These results, taken together with previous in vitro and clinical studies with ACR, suggest that this agent may be useful in the chemoprevention and therapy of he...

متن کامل

Posttranscriptional stabilization underlies p53-independent induction of p21WAF1/CIP1/SDI1 in differentiating human leukemic cells.

p21WAF/CIP1/SDI1 is a recently identified gene expressed in cells harboring wild-type but not mutant p53 gene. It encodes a nuclear protein of 21 kD which inhibits cyclin-dependent kinase activity. Constitutive p21WAF1/CIP1/SDI1 mRNA expression was detected in neoplastic cells from patients with various hematological malignancies as well as in normal bone marrow mononuclear cells and in myeloid...

متن کامل

 - TGF ، سنتز آلفا ـ 1 ـ آنتی تریپسین را در سلولهای هپاتومای انسانی (HepG2)

Cytokines protein or glycoproteins synthesized by a wide range of cell types including lymphocytes, macrophages, platelets, and monocytes. Cytokines induse synthesis of acute phase protein in hepatocytes. So far eight cytokines has been shown can induce acute phase protein synthesis in hepatocyte and hepatoma cell culture. There are evidences that transforming growth factor-alpha (TGF-a) secr...

متن کامل

Synergistic effects of acyclic retinoid and OSI-461 on growth inhibition and gene expression in human hepatoma cells.

Hepatoma is one of the most frequently occurring cancers worldwide. However, effective chemotherapeutic agents for this disease have not been developed. Acyclic retinoid, a novel synthetic retinoid, can reduce the incidence of postsurgical recurrence of hepatoma and improve the survival rate. OSI-461, a potent derivative of exisulind, can increase intracellular levels of cyclic GMP, which leads...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2014