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Tumour Biol. 2016 Oct 05; doi: 10.1007/s13277-016-5333-2. Epub 2016 Oct 05.

Cancer/testis antigens as molecular drug targets using network pharmacology.

Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine

Anuj Kumar, Drista Sharma, M L Aggarwal, K M Chacko, Tarun Kumar Bhatt

Affiliations

  1. Shriram Institute for Industrial Research, 19, University Road Delhi, Delhi, 110 007, India. [email protected].
  2. Department of Biotechnology, Central University of Rajasthan, NH-8, Bandarsindri, Rajasthan, 305801, India.
  3. Shriram Institute for Industrial Research, 19, University Road Delhi, Delhi, 110 007, India.
  4. Department of Biotechnology, Central University of Rajasthan, NH-8, Bandarsindri, Rajasthan, 305801, India. [email protected].

PMID: 27709548 DOI: 10.1007/s13277-016-5333-2

Abstract

Present chemotherapeutic drugs have limited efficacy and severe side effects. Considering the complexity of cancer, an effective strategy is necessary to discover multiple new drug targets. Cancer/testis antigens are vital for cancer cell progression. We have performed a computational network analysis of cancer/testis antigens and assessed these antigens as drug targets. During this analysis, protein interaction network of 700 human CT antigens was investigated. CT antigen network consisted of eight independent components. Four major hubs and two minor hubs were identified that play nodal role in the flow of information across the largest network. We have predicted 30 potential drug targets by analysing several topological parameters such as betweenness centrality, cluster coefficient and probable protein complexes. Structural and functional roles of potential drug targets have also been anatomized. Analysis of the CT antigen network enables us to pinpoint a set of candidate proteins that if targeted could be detrimental for cancerous cell without affecting any normal cell. The list of putative proteins is a starting point for experimental validation and may help further in the discovery of new anticancer drug targets.

Keywords: Anticancer targets; Cancer; Cancer/testis antigens; Protein interaction network

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