Cytotoxicity activity of extracts and compounds from Commiphora myrrha resin against human gynecologic cancer cells

نویسندگان

  • Shulan Su
  • Tuanjie Wang
  • Ting Chen
  • Jin-ao Duan
  • Li Yu
  • Yuping Tang
چکیده

The purpose of this report is to explore the cytotoxicity effects of extracts and compounds from Commiphora myrrha resin on human gynecologic cancer cells. The results showed that AE (85% EtOH extract), and petroleum ether extract (PE) from C. myrrha significantly inhibited cell proliferation of A2780, SK-OV-3, and Shikawa with dose-dependent relation in vitro. The inhibitory effects of AE and PE on A2708 cell were strongest and the IC50s were 15.8 and 26.91 μg/ml, respectively. The IC50s of AE and PE on Shikawa cell lines were 20.73 and 26.63 μg/ml respectively. Furthermore, nine compounds were isolated and identified from bio-activity guided separation fraction, and were determined the cytotoxicity activity on A2780, SK-OV-3, SiHa cells and Shikawa cells. Compounds 14, 6 and 7 are isolated from this genus for the first time. The compound 6 and 7 exhibited obvious cytotoxicty effects on A2780, SK-OV-3, and Shikawa cancer cells with dose-dependent relationship. The antiprolifirative activity of compound 6 on A2780 cells was most obviously with IC50 46.89 μM. The compound 7 with IC50 26.93 μM inhibited cell growth of SK-OV-3 cells. The determined compounds have never shown antiproliferative activities on SiHa cells. These findings suggested that extracts and compounds from myrrh could be useful for preventing and treating human gynecologic cancer disease.

برای دانلود رایگان 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

Short communication TOXICITY STUDY IN MICE OF RESINS OF THREE COMMIPHORA SPECIES

Acute toxicity studies of crude extracts of resins of Commiphora myrrha, C. guidottii and C. erlangeriana, and pure compounds isolated from C. erlangeriana were conducted on Swiss albino mice. The extract from C. erlangeriana had a mean LD50 of 410 mg/kg body weight. However the extracts from C. myrrha and C. guidotti were not toxic at the doses tested. The pure compound isolated from C. erlang...

متن کامل

Phytochemical Study of the Biologically Active Fractions of the Oleo-gum-resins of Boswellia carteri and Commiphora myrrha

The petroleum ether extract of the oleo-gum-resin of Boswellia carteri Bird., the chloroformic successive extract of the oleo-gum-resin of Commiphora myrrha Engl. as well as the prepared volatile contents from both resins showed significant anti-inflammatory activity in carragennan-induced edema in rats. Phytochemical investigation of the volatile fractions was carried out using GC/MS and revea...

متن کامل

Anti-inflammatory Activity of Some Traditional Medicinal Plants

The ethanol extract of roots, fruits and roots of solanum indicum and saccharum munja respectively and water soluble resin of commiphora myrrha were studied for antiinflammatory activity against carrageenin induced oedema in rats, the significant antiinflammatory activity were found in former two plants will slight anti inflammatory activity was observed in latter plant.

متن کامل

Gummosin, a sesquiterpene coumarin from Ferula assa-foetida is preferentially cytotoxic to human breast and prostate cancer cell lines

Objective: The present study was conducted to find cytotoxic compounds from oleo-gum-resin of Ferula assa-foetida (asafoetida). Materials and Methods: A di...

متن کامل

Cycloartan-24-ene-1α,2α,3β-triol, a cycloartane-type triterpenoid from the resinous exudates of Commiphora myrrha, induces apoptosis in human prostatic cancer PC-3 cells.

Plant-derived antitumor drugs are currently used in chemotherapy. Cycloartane triterpenoids have shown a cytotoxic effect on human prostate cancer cells. The aim of the present study was to isolate a cycloartane triterpenoid from Commiphora myrrha and evaluate its anticancer potential. Cycloartan-24-ene-1α,2α,3β-triol (MY-1) was isolated from Commiphora myrrha, and its structure was determined ...

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

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2011