Bacterial proteins and peptides in cancer therapy

Cancer is one of the most deadly diseases worldwide. In the last three decades many efforts have been made focused on understanding how cancer grows and responds to drugs. The dominant drug-development paradigm has been the “one drug, one target.” Based on that, the two main targeted therapies developed to combat cancer include the use of tyrosine kinase inhibitors and monoclonal antibodies. Development of drug resistance and side effects represent the major limiting factors for their use in cancer treatment. Nowadays, a new paradigm for cancer drug discovery is emerging wherein multi-targeted approaches gain ground in cancer therapy. Therefore, to overcome resistance to therapy, it is clear that a new generation of drugs is urgently needed. Here, regarding the concept of multi-targeted therapy, we discuss the challenges of using bacterial proteins and peptides as a new generation of effective anti-cancer drugs.

[1]  C. Beattie,et al.  A first-in-class, first-in-human phase I trial of p28, a non-HDM2-mediated peptide inhibitor of p53 ubiquitination in patients with metastatic refractory solid tumors. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[2]  J. Shaji,et al.  Protein and Peptide Drug Delivery: Oral Approaches , 2008, Indian journal of pharmaceutical sciences.

[3]  R. Jenkins,et al.  Effective intravenous therapy for neurodegenerative disease with a therapeutic enzyme and a peptide that mediates delivery to the brain. , 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

[4]  J. Reichert,et al.  Future directions for peptide therapeutics development. , 2013, Drug discovery today.

[5]  André F. Vieira,et al.  P-cadherin role in normal breast development and cancer. , 2011, The International journal of developmental biology.

[6]  A. Rehemtulla,et al.  Destabilization of the Epidermal Growth Factor Receptor (EGFR) by a Peptide That Inhibits EGFR Binding to Heat Shock Protein 90 and Receptor Dimerization*♦ , 2013, The Journal of Biological Chemistry.

[7]  Mindy I. Davis,et al.  A quantitative analysis of kinase inhibitor selectivity , 2008, Nature Biotechnology.

[8]  S. Manna,et al.  Glioblastoma Multiforme: Novel Therapeutic Approaches , 2012, ISRN neurology.

[9]  A. Mehta,et al.  Pivotal trial with plant cell-expressed recombinant glucocerebrosidase, taliglucerase alfa, a novel enzyme replacement therapy for Gaucher disease. , 2011, Blood.

[10]  C. Beattie,et al.  Noncationic peptides obtained from azurin preferentially enter cancer cells. , 2009, Cancer research.

[11]  M. Wangpaichitr,et al.  Arginine Deiminase and Cancer Therapy , 2010 .

[12]  D. Schlaepfer,et al.  Multiple connections link FAK to cell motility and invasion. , 2004, Current opinion in genetics & development.

[13]  A. Duhme-Klair,et al.  The background, discovery and clinical development of BCR-ABL inhibitors. , 2013, Drug discovery today.

[14]  Neha Kohli,et al.  Oral delivery of bioencapsulated proteins across blood-brain and blood-retinal barriers. , 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

[15]  D. Majumdar,et al.  A cell penetrating peptide derived from azurin inhibits angiogenesis and tumor growth by inhibiting phosphorylation of VEGFR-2, FAK and Akt , 2011, Angiogenesis.

[16]  M. Bucciantini,et al.  Interaction of an anticancer peptide fragment of azurin with p53 and its isolated domains studied by atomic force spectroscopy , 2011, International journal of nanomedicine.

[17]  E. Arbit,et al.  Glucose-Reducing Effect of the ORMD-0801 Oral Insulin Preparation in Patients with Uncontrolled Type 1 Diabetes: A Pilot Study , 2013, PloS one.

[18]  R. Verma,et al.  Therapeutic potential of anticancer immunotoxins. , 2011, Drug discovery today.

[19]  D. Schlaepfer,et al.  Integrin-regulated FAK-Src signaling in normal and cancer cells. , 2006, Current opinion in cell biology.

[20]  Arsenio M. Fialho,et al.  The Role and Importance of Intellectual Property Generation and Protection in Drug Development , 2010 .

[21]  A. Chakrabarty,et al.  Overcoming drug resistance in multi-drug resistant cancers and microorganisms , 2012, Bioengineered.

[22]  A. Chakrabarty,et al.  Internalization of bacterial redox protein azurin in mammalian cells: entry domain and specificity , 2005, Cellular microbiology.

[23]  E. Avizienyte,et al.  Src and FAK signalling controls adhesion fate and the epithelial-to-mesenchymal transition. , 2005, Current opinion in cell biology.

[24]  J. Guan,et al.  Focal adhesion kinase: a prominent determinant in breast cancer initiation, progression and metastasis. , 2010, Cancer letters.

[25]  A. Mercurio,et al.  Neuropilin-2 regulates α6β1 integrin in the formation of focal adhesions and signaling , 2012, Journal of Cell Science.

[26]  C. Beattie,et al.  A 28-Amino-Acid Peptide Fragment of the Cupredoxin Azurin Prevents Carcinogen-Induced Mouse Mammary Lesions , 2010, Cancer Prevention Research.

[27]  G. Kim,et al.  The Bacterial Protein Azurin Enhances Sensitivity of Oral Squamous Carcinoma Cells to Anticancer Drugs , 2011, Yonsei medical journal.

[28]  A. Chakrabarty,et al.  Cupredoxin-cancer interrelationship: azurin binding with EphB2, interference in EphB2 tyrosine phosphorylation, and inhibition of cancer growth. , 2007, Biochemistry.

[29]  R. A. Etten,et al.  Molecular mechanisms of cardiotoxicity of tyrosine kinase inhibition , 2007, Nature Reviews Cancer.

[30]  Carlos L. Arteaga,et al.  Treatment of HER2-positive breast cancer: current status and future perspectives , 2012, Nature Reviews Clinical Oncology.

[31]  Sten Ohlson,et al.  Designing transient binding drugs: a new concept for drug discovery. , 2008, Drug discovery today.

[32]  H. Hua,et al.  Matrix metalloproteinases in tumorigenesis: an evolving paradigm , 2011, Cellular and Molecular Life Sciences.

[33]  G. Demetri,et al.  Molecular basis for sunitinib efficacy and future clinical development , 2007, Nature Reviews Drug Discovery.

[34]  David Zurakowski,et al.  Cardiotoxicity associated with tyrosine kinase inhibitor sunitinib , 2007, The Lancet.

[35]  A. Chakrabarty,et al.  Promiscuous Anticancer Drugs from Pathogenic Bacteria: Rational Versus Intelligent Drug Design , 2010 .

[36]  D. Majumdar,et al.  A peptide fragment of azurin induces a p53-mediated cell cycle arrest in human breast cancer cells , 2009, Molecular Cancer Therapeutics.

[37]  Ljiljana Paša-Tolić,et al.  Identification of a Putative Protein Profile Associated with Tamoxifen Therapy Resistance in Breast Cancer*S⃞ , 2009, Molecular & Cellular Proteomics.

[38]  E. Sauter,et al.  Increased shedding of soluble fragments of P‐cadherin in nipple aspirate fluids from women with breast cancer , 2008, Cancer science.

[39]  A. Chakrabarty,et al.  Beyond host-pathogen interactions: microbial defense strategy in the host environment. , 2007, Current opinion in biotechnology.

[40]  J. Bergh,et al.  Hurdles in anticancer drug development from a regulatory perspective , 2012, Nature Reviews Clinical Oncology.

[41]  M. Moore,et al.  Advanced pancreatic carcinoma: current treatment and future challenges , 2010, Nature Reviews Clinical Oncology.

[42]  Funda Meric-Bernstam,et al.  Targeting the mTOR signaling network for cancer therapy. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[43]  Carmen Jerónimo,et al.  P-Cadherin Overexpression Is an Indicator of Clinical Outcome in Invasive Breast Carcinomas and Is Associated with CDH3 Promoter Hypomethylation , 2005, Clinical Cancer Research.

[44]  A. Chakrabarty,et al.  Apoptosis or growth arrest: Modulation of tumor suppressor p53's specificity by bacterial redox protein azurin. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[45]  Yunlei Zhang,et al.  Escherichia coli Nissle 1917 Targets and Restrains Mouse B16 Melanoma and 4T1 Breast Tumors through Expression of Azurin Protein , 2012, Applied and Environmental Microbiology.

[46]  A. Wolff,et al.  Treatment of HER 2-positive Breast Cancer , 2015 .

[47]  F. Milletti,et al.  Cell-penetrating peptides: classes, origin, and current landscape. , 2012, Drug discovery today.

[48]  Xin Huang,et al.  Bacterial redox protein azurin induce apoptosis in human osteosarcoma U2OS cells. , 2005, Pharmacological research.

[49]  W. McBride,et al.  Small Azurin Derived Peptide Targets Ephrin Receptors for Radiotherapy , 2011, International Journal of Peptide Research and Therapeutics.

[50]  N. Bernardes,et al.  The Bacterial Protein Azurin Impairs Invasion and FAK/Src Signaling in P-Cadherin-Overexpressing Breast Cancer Cell Models , 2013, PloS one.

[51]  A. Chakrabarty,et al.  Patent controversies and court cases , 2012, Cancer biology & therapy.

[52]  Manuel A. S. Santos,et al.  High-throughput molecular profiling of a P-cadherin overexpressing breast cancer model reveals new targets for the anti-cancer bacterial protein azurin. , 2014, The international journal of biochemistry & cell biology.

[53]  X. Zheng,et al.  Targeting the mTOR kinase domain: the second generation of mTOR inhibitors. , 2011, Drug discovery today.

[54]  D. Majumdar,et al.  A first-in-class, first-in-human, phase I trial of p28, a non-HDM2-mediated peptide inhibitor of p53 ubiquitination in patients with advanced solid tumours , 2013, British Journal of Cancer.

[55]  A. S. A. Don,et al.  Recent clinical trials of mTOR-targeted cancer therapies. , 2011, Reviews on recent clinical trials.