Somasundaram Thirugnanasambandam Somasundaram

Dr. Somasundaram Thirugnanasambandam Somasundaram


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 February 2010 in Current Microbiology
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Journal Article
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KAK. M. Alagappan
K. M. Alagappan
Balaraman DeivasigamaniBalaraman Deivasigamani
Balaraman Deivasigamani
SSSomasundaram Thirugnanasambandam Somasundaram
Somasundaram Thirugnanasambandam Somasundaram
KSKumaran Subramanian
Kumaran Subramanian

25 June 2002 in British Journal of Cancer
Verified
Journal Article
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PGP Giridharan
P Giridharan
SSSomasundaram Thirugnanasambandam Somasundaram
Somasundaram Thirugnanasambandam Somasundaram
KPK Perumal
K Perumal
RVR A Vishwakarma
R A Vishwakarma
NKN P Karthikeyan
N P Karthikeyan
ABA Balakrishnan
A Balakrishnan
Conventional solvent fractionation and bioactivity based target assays were used to identify a new anti-cancer molecule from Phyllanthus urinaria, a herbal medicinal plant used in South India. At each step of the purification process the different fractions that were isolated were tested for specific anti-proliferative activity by assays measuring the inhibition of [3H]thymidine incorporation, and trypan blue drug exclusion. The ethyl acetate fraction that contained the bioactivity was further purified and resolved by HPLC on a preparative column. The purity of each of the fractions and their bioactivity were checked. Fraction 3 demonstrated a single spot on TLC and showed maximum anti-proliferative activity. This fraction was further purified and the structure was defined as 7′-hydroxy-3′,4′,5,9,9′-pentamethoxy-3,4-methylene dioxy lignan using NMR and mass spectrometry analysis. The pure compound and the crude ethyl acetate fraction which showed anti-proliferative activities were examined for ability to target specific markers of apoptosis like bcl2, c-myc and caspases and for effects on telomerase. Four specific cancer cell lines HEp2, EL-1 monocytes, HeLa and MCP7 were used in this study. The results indicate that 7′-hydroxy-3′,4′,5,9,9′-pentamethoxy-3,4-methylene dioxy lignan was capable of inhibiting telomerase activity and also could inhibit bcl2 and activate caspase 3 and caspase 8 whose significance in the induction of apoptosis is well known. We believe that this compound could serve as a valuable chemotherapeutic drug after further evaluations.


29 June 2019 in Biological Trace Element Research
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SRSrinath Rajeswaran
Srinath Rajeswaran
SSSomasundaram Thirugnanasambandam Somasundaram
Somasundaram Thirugnanasambandam Somasundaram
NDNaresh Kumar Dewangan
Naresh Kumar Dewangan
RMRajesh Kannan Moorthy
Rajesh Kannan Moorthy
SKSaravanan Kandasamy
Saravanan Kandasamy
RVRavikumar Vilwanathan
Ravikumar Vilwanathan

1 March 2015 in International Journal of Biological Macromolecules
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Journal Article
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CDCaroline R. Delma
Caroline R. Delma
SSSomasundaram Thirugnanasambandam Somasundaram
Somasundaram Thirugnanasambandam Somasundaram
GSGuru Prasad Srinivasan
Guru Prasad Srinivasan
MKMd Khursheed
Md Khursheed
MBMurali D. Bashyam
Murali D. Bashyam
Natarajan AravindanNatarajan Aravindan
Natarajan Aravindan

6 April 2021 in Journal of Microbiology and Biotechnology
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SLSivakumar Lingappa
Sivakumar Lingappa
MSMuthugounder Subramanian Shivakumar
Muthugounder Subramanian Shivakumar
TMThamilarasan Manivasagam
Thamilarasan Manivasagam
SSSomasundaram Thirugnanasambandam Somasundaram
Somasundaram Thirugnanasambandam Somasundaram
PSPalaniappan Seedevi
Palaniappan Seedevi
Sivakumar Lingappa, Muthugounder Subramanian Shivakumar, Thamilarasan Manivasagam, Somasundaram Thirugnanasambandan Somasundaram, and Palaniappan Seedevi. J. Microbiol. Biotechnol. 2021;31:867-74. https://doi.org/10.4014/jmb.2101.01002