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Biochemistry & Molecular Biology Journal

ISSN: 2471-8084

Internat i ona l Conference on

Biotechnology, Biomarkers

& Systems Biology

M a r c h 0 4 - 0 5 , 2 0 1 9

Am s t e r d a m , N e t h e r l a n d s

Biotechnology, Biomarkers & Systems Biology 2019

Background:

Cancer is one of the most important problems in the world. Today Enzymes have been intensively studied as a

source of antitumor compounds. L-Asparaginase (L-ASNase) is one of the most therapeutic enzyme which used for the cancer

therapy. The attendance of L-ASNase has been reported in various organisms, containing animals, plants, and microorganisms

(bacteria, fungi, algae, yeast, and actinomycetes) except humans. In this study we used L-ASNase enzyme which isolated from

Yarrowia yeast.

Methods:

In this study, Raji, MCF7 and A549 cell lines were cultured in RPMI 1640 with 10% FBS and 5% of CO2 condition.

Cytotoxic effects of yeasts L-asparaginase was assessed by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT)

assay. Then, flow cytometry assay was exploited to measure cell death and apoptosis stage.

Results:

According to our findings, yeasts L-asparaginase can inhibit cell growth in a time and dose dependent manner. Flow

cytometry assay result showed that yeasts L-asparaginase was able to induce apoptosis in Raji, MCF7 and A549 cell lines. The

apoptosis of raji cells is more than other cell lines and A549 is more than MCF-7.

Conclusion:

Our results showed that yeasts L-asparaginase could successfully induce apoptosis in Raji, MCF7 and A549 cell

lines. Therefore, it could be used as a novel and safe therapeutic candidate for cancer treatment.

perzhad.mazloumi@gmail.com

Yeasts L-asparaginase inhibits cell growth

and induces apoptosis of acute lymphoblastic

leukaemia (Raji), breast cancer (MCF-7) and lung

cancer (A549) cells in in-vitro system

Sahand Mazloum Ravasan

1

, Elaheh Madadi Hiyagh

1

, Farshad

Darvish

2

, Ahad Mokhtarzadeh

1

and Behzad Baradaran

1

1

Immunology Research Center-Tabriz University of Medical Sciences, Iran

2

University of Maragheh, Iran

Biochem Mol biol J 2019, Volume:5

DOI: 10.21767/2471-8084-C1-024