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Cancer is a group of diseases that arise from uncontrolled growth, spread of
an abnormal cell and can result in death. The inefficiency (Tong
et al
, 1995)
to treat several distinct classes of tumours led researchers to source for potential
natural-based therapeutic compounds. Many Botanists (Etta, 2008) believed that
the extract of
P. niruri,
(30 - 40 cm in height)
originated
from India by late of 1980s
showed pharmacological, clinical efficacy against viral Hepatitis B (Padma
et al
.,
1999; Paranjpe, 2001; Blumberg
et al
., 1990; Venkateswaran
et al
., 1987) anti-
bacterial activity (Mazumder
et al
., 2006); Kloucek
et al
., 2005), anti-hepatotoxic or
liver-protecting activity (Houghton
et al
., 1996; Rajeshkumar
et al
., 2000; Jeena et
al., 1999), as well as anti-tumor and anti-carcinogenic properties (Rajeshkumar
et
al
., 2001). In addition, it also exhibits hypoglycaemia properties (Mazunder
et al
.,
2005; Raphael
et al
., 2002).
The objective of the present study determines the cytotoxic effect of
Phyllanthus
extracts (aqueous and methanol) on growth inhibition against skin melanoma and
prostate cancer cells in their cell cycle could partially explain its mode of activity
and proliferation effect with apoptosis induction and cell cycle modulation. From the
results,
Phyllanthus
plant appears to possess antiproliferative (cytotoxic) properties
against breast, lung, melanoma and prostate cancer cells with IC
50
values ranging
between 150�400 �?¼g/ml for the aqueous extract and 50�150 �?¼g/ml for the metha
-
nolic extract which were determined using the MTS reduction assay. In compari
-
son, the plant extracts did not show significant cytotoxicity on normal human cells
(breast, lung, skin (CRL-2565) and prostate (RWPE-1) cells). This indicates that
Phyllanthus
is one step closer to being a suitable candidate for the development of
effective anticancer drugs.
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