Dr. George Kulik

Associate Professor of Cancer Biology

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Bios
Dr. Kulik earned his graduate degree at the Institute of Experimental Pathology in Kiev, Ukraine and obtained post-doctoral training in the Imperial Cancer Research Fund (London, UK) and University of Virginia (Charlottesville, USA).  As a post-doctoral fellow Dr. Kulik identified for the first time the critical role of the PI3K/AKT signaling module in apoptosis inhibition by IGF-1.  The importance of PI3K/AKT signaling for cell survival was later confirmed in numerous publications and now this signaling pathway is a major focus of leading pharmaceutical companies.
His laboratory investigated the mechanisms by which cancer cell signaling pathways become integrated into a robust regulatory network, and the ways this knowledge can be utilized to improve cancer diagnosis and therapy. Dr. Kulik group has made discoveries that provide insight into the linkage between emotional stress of an individual and the regulation of anti-apoptotic pathways in tumors.  
Research program of Dr. Kulik integrates a variety of methods ranging from molecular biology and proteomics to transgenic mouse models of prostate cancer, bioluminescent imaging and behavioral studies in mice.  Basic science findings on signaling network that controls apoptosis in prostate cancer cells made in his laboratory became a basis for translational projects that aim to examine effects of psychological stress on activation of neuroendocrine pathways in prostates of men and on prostate cancer progression and develop prostate tumor-specific inhibitors of anti-apoptotic signaling pathways.  These projects are conducted in collaborations with experts in medicinal chemistry, in silico drug design, toxin targeted therapies, systems biology and clinical urology.
3_kulik_cv_alf.pdf (332.34 KB)

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Publications

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Behavioral stress accelerates prostate cancer development in mice

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Behavioral stress accelerates prostate cancer development in mice. (2013). Behavioral stress accelerates prostate cancer development in mice. The Journal Of Clinical Investigation, 123, 874–886.

Combination of the PI3K inhibitor ZSTK474 with a PSMA-targeted immunotoxin accelerates apoptosis and regression of prostate cancer

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Combination of the PI3K inhibitor ZSTK474 with a PSMA-targeted immunotoxin accelerates apoptosis and regression of prostate cancer. (2013). Combination of the PI3K inhibitor ZSTK474 with a PSMA-targeted immunotoxin accelerates apoptosis and regression of prostate cancer. Neoplasia, 15, 1172–IN32.

Cooperation between< i> Dmp1</i> Loss and Cyclin D1 Overexpression in Breast Cancer

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Cooperation between< i> Dmp1 Loss and Cyclin D1 Overexpression in Breast Cancer. (2013). Cooperation between< i> Dmp1 Loss and Cyclin D1 Overexpression in Breast Cancer. The American Journal Of Pathology, 183, 1339–1350.

Dimeric DNA aptamer complexes for high-capacity–targeted drug delivery using pH-sensitive covalent linkages

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Dimeric DNA aptamer complexes for high-capacity–targeted drug delivery using pH-sensitive covalent linkages. (2013). Dimeric DNA aptamer complexes for high-capacity–targeted drug delivery using pH-sensitive covalent linkages. Molecular Therapy—Nucleic Acids, 2, e107.

Recent syntheses of PI3K/Akt/mTOR signaling pathway inhibitors

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Recent syntheses of PI3K/Akt/mTOR signaling pathway inhibitors. (2013). Recent syntheses of PI3K/Akt/mTOR signaling pathway inhibitors. Bioorganic & Medicinal Chemistry, 21, 4063–4091.

Behavioral stress accelerates prostate cancer development in mice.

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Behavioral stress accelerates prostate cancer development in mice. (2013). Behavioral stress accelerates prostate cancer development in mice. J Clin Invest, 123, 874–886.

BAD Dephosphorylation and Decreased Expression of MCL-1 Induce Rapid Apoptosis in Prostate Cancer Cells

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BAD Dephosphorylation and Decreased Expression of MCL-1 Induce Rapid Apoptosis in Prostate Cancer Cells. (2013). BAD Dephosphorylation and Decreased Expression of MCL-1 Induce Rapid Apoptosis in Prostate Cancer Cells. Plos One, 8, e74561.

Synthesis and characterization of a novel prostate cancer-targeted phosphatidylinositol-3-kinase inhibitor prodrug

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Synthesis and characterization of a novel prostate cancer-targeted phosphatidylinositol-3-kinase inhibitor prodrug. (2012). Synthesis and characterization of a novel prostate cancer-targeted phosphatidylinositol-3-kinase inhibitor prodrug. Journal Of Medicinal Chemistry, 55, 8038–8046.

Large Magnetic Entropy Change in La< SUB> 0.55</SUB> Ce< SUB> 0.2</SUB> Ca< SUB> 0.25</SUB> MnO₃ Perovskite

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Large Magnetic Entropy Change in La< SUB> 0.55 Ce< SUB> 0.2 Ca< SUB> 0.25 MnO₃ Perovskite. (2010). Large Magnetic Entropy Change in La< SUB> 0.55 Ce< SUB> 0.2 Ca< SUB> 0.25 MnO₃ Perovskite. 한국자기학회 학술연구발표회 논문개요집, 277–277.

Expression of the Bcl-2 protein BAD promotes prostate cancer growth

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Expression of the Bcl-2 protein BAD promotes prostate cancer growth. (2009). Expression of the Bcl-2 protein BAD promotes prostate cancer growth. Plos One, 4, e6224.

Epinephrine protects cancer cells from apoptosis via activation of cAMP-dependent protein kinase and BAD phosphorylation

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Epinephrine protects cancer cells from apoptosis via activation of cAMP-dependent protein kinase and BAD phosphorylation. (2007). Epinephrine protects cancer cells from apoptosis via activation of cAMP-dependent protein kinase and BAD phosphorylation. Journal Of Biological Chemistry, 282, 14094–14100.

Modulation of prostate cancer genetic risk by omega-3 and omega-6 fatty acids

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Modulation of prostate cancer genetic risk by omega-3 and omega-6 fatty acids. (2007). Modulation of prostate cancer genetic risk by omega-3 and omega-6 fatty acids. The Journal Of Clinical Investigation, 117, 1866–1875.

Diverse anti-apoptotic signaling pathways activated by VIP, EGF and PI3K in prostate cancer cells converge on BAD

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Diverse anti-apoptotic signaling pathways activated by VIP, EGF and PI3K in prostate cancer cells converge on BAD. (2006). Diverse anti-apoptotic signaling pathways activated by VIP, EGF and PI3K in prostate cancer cells converge on BAD. Journal Of Biological Chemistry.

Diverse antiapoptotic signaling pathways activated by vasoactive intestinal polypeptide, epidermal growth factor, and phosphatidylinositol 3-kinase in prostate cancer cells converge on BAD

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Diverse antiapoptotic signaling pathways activated by vasoactive intestinal polypeptide, epidermal growth factor, and phosphatidylinositol 3-kinase in prostate cancer cells converge on BAD. (2006). Diverse antiapoptotic signaling pathways activated by vasoactive intestinal polypeptide, epidermal growth factor, and phosphatidylinositol 3-kinase in prostate cancer cells converge on BAD. Journal Of Biological Chemistry, 281, 20891–20901.

Epidermal growth factor protects prostate cancer cells from apoptosis by inducing BAD phosphorylation via redundant signaling pathways

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Epidermal growth factor protects prostate cancer cells from apoptosis by inducing BAD phosphorylation via redundant signaling pathways. (2006). Epidermal growth factor protects prostate cancer cells from apoptosis by inducing BAD phosphorylation via redundant signaling pathways. Journal Of Biological Chemistry, 281, 27367–27377.

Smac is required for cytochrome c-induced apoptosis in prostate cancer LNCaP cells

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Smac is required for cytochrome c-induced apoptosis in prostate cancer LNCaP cells. (2002). Smac is required for cytochrome c-induced apoptosis in prostate cancer LNCaP cells. Cancer Research, 62, 18–23.

Tumor necrosis factor $\alpha$ induces BID cleavage and bypasses antiapoptotic signals in prostate cancer LNCaP cells

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Tumor necrosis factor $\alpha$ induces BID cleavage and bypasses antiapoptotic signals in prostate cancer LNCaP cells. (2001). Tumor necrosis factor $\alpha$ induces BID cleavage and bypasses antiapoptotic signals in prostate cancer LNCaP cells. Cancer Research, 61, 2713–2719.

Antiapoptotic Signaling in LNCaP Prostate Cancer Cells A Survival Signaling Pathway Independent of Phosphatidylinositol 3'-Kinase and Akt/Protein Kinase B

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Antiapoptotic Signaling in LNCaP Prostate Cancer Cells A Survival Signaling Pathway Independent of Phosphatidylinositol 3'-Kinase and Akt/Protein Kinase B. (1999). Antiapoptotic Signaling in LNCaP Prostate Cancer Cells A Survival Signaling Pathway Independent of Phosphatidylinositol 3'-Kinase and Akt/Protein Kinase B. Cancer Research, 59, 1449–1453.

Akt-dependent and-independent survival signaling pathways utilized by insulin-like growth factor I

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Akt-dependent and-independent survival signaling pathways utilized by insulin-like growth factor I. (1998). Akt-dependent and-independent survival signaling pathways utilized by insulin-like growth factor I. Molecular And Cellular Biology, 18, 6711–6718.

Antiapoptotic signalling by the insulin-like growth factor I receptor, phosphatidylinositol 3-kinase, and Akt.

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Antiapoptotic signalling by the insulin-like growth factor I receptor, phosphatidylinositol 3-kinase, and Akt. (1997). Antiapoptotic signalling by the insulin-like growth factor I receptor, phosphatidylinositol 3-kinase, and Akt. Molecular And Cellular Biology, 17, 1595–1606.

Src phosphorylates the insulin-like growth factor type I receptor on the autophosphorylation sites requirement for transformation by src

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Src phosphorylates the insulin-like growth factor type I receptor on the autophosphorylation sites requirement for transformation by src. (1996). Src phosphorylates the insulin-like growth factor type I receptor on the autophosphorylation sites requirement for transformation by src. Journal Of Biological Chemistry, 271, 31562–31571.

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Classes

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BIO 346, Biochemistry I

Semester Schedule:

The schedule is subject to change according to the need of the class and the instructor, as determined by the instructor.

date

chapter #

                                                topic

Sept 1

 

Introduction

Sept 3

chapter 1

The foundations of biochemistry (introduction, 1.1 cellular foundations)

 Sept 8

chapter 1

The foundations of biochemistry (1.2 chemical foundations)

 

Sept 10

chapter 1

The foundations of biochemistry

(1.3 physical , 1.4 genetic, 1.5 evolutionary)

Sept 12

Lab 0

Basics of safe techniques

 Sept 15

chapter 2

Water (2.1 Weak Interactions in aqueous systems)

Sept 17

chapter 2

Water  (2.2 Ionization of water, weak acids and weak bases)

Sept 19

Lab 1

Titration curves of amino acids

 Sept 22

chapter 2

Water

(2.3 Buffering; 2.4 Water as reactant; 2.5 The fitness of water for living)

Sept 24

chapter 3

Amino acids, peptides and proteins (3.1  Amino acids)

Sept 26

Lab 2

The absorbance curves of two colored compounds

Sept 29

chapter 3

Amino acids, peptides and proteins

 (3.2  Peptide and proteins; 3.3 Working with  proteins)

Oct 1

chapter 3

Amino acids, peptides and proteins (4.3 Primary structure)

Oct 3

Lab 3

General properties of amino acid

 Oct 6

chapter 4

Protein tertiary and quaternary structures

Oct 8

 

Midterm examination I

 

 

Eid Aladha Holiday (Oct 11-Oct 22)

Oct 22

chapter 5

Protein function (5.1 Reversible binding of a protein to a ligand)

Oct 24

Lab 4

Separation of amino acid by paper chromatography

 Oct 27

chapter 5

Protein function (5.3 Protein interactions modulated by chemical energy)

Oct 29

chapter 6

Enzymes (6.1 Introduction to enzymes; 6.2 How enzymes work)

Oct 31

Lab 5

General properties of protein

 Nov 3

chapter 6

Enzymes

(6.3 Enzyme kinetics as an approach to understanding mechanism)

Nov 5

chapter 6

Enzymes

(6.4 Examples of enzymatic reactions; 6.5 Regulatory enzymes) 

Nov 7

Lab 6

Quantitation of proteins

 Nov 10

chapter 8

Nucleotides and nucleic acids

(8.1 Some basics; 8.2 Nucleic acid structure)

Nov 12

chapter 8

Nucleotides and nucleic acids

(8.3 Nucleic acid chemistry; 8. 4 Other functions)

Nov 14

Lab 7

Preparation of an enzyme extraction

 Nov 17

chapter 0

Lipids.  (10.1 Storage Lipids; 10.2 Structural lipids in membranes)

Nov 19

chapter 10

Lipids

(10.3  Lilpids as signals, cofactors and pigments; 10.4 Working with lipids)

Nov 21

Lab 8

General properties of lipids

 Nov 24

 

Midterm examination II

Nov 26

chapter 11

Biological membranes and transport

(11.1 Composition and architecture of membranes)

Nov 28

Lab 9

General test for carbohydrate

 Dec 1

chapter 11

Biological membranes and transport

(1.3  Solute transport across membranes)

Dec 3

chapter 12

Biosignaling (12.1 General features of signal transduction )

 Dec 8

chapter 12

Biosignaling 

(12.2 G Protein-Coupled Receptors and second messengers)

Dec 10

chapter 12

Biosignaling  (12.3 Receptor Tyrosine Kinases)

 Dec 15

chapter 13

Bioenergetics and biochemical reaction types

(Introduction;  13.1 Bioenergetics and thermodynamics )

Dec 17

chapter 13

Bioenergetics and biochemical reaction types

(13.2 Biochemical logic and common biochemical reactions )

Dec 22

chapter 13

Bioenergetics and biochemical reaction types

(13.3 Phosphoryl group transfers and ATP)

Dec 24

 

Midterm Examination III         

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BIO224 Human Physiology and Anatomy

The textbook for the BIO224 "Human Physiology and Anatomy" 2nd year biomedical science major course, spring semester, 4 credit hours, of which 1 crh for labs: Title: Essentials of Human Anatomy & Physiology with MasteringA&P, 10th Edition, 2011 Author: Elaine N. Marieb Publisher: Benjamin Cummings ISBN-10: 0321732022 ISBN-13: 978-0321732026 Normal 0 false false false EN-GB X-NONE X-NONE /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin-top:0cm; mso-para-margin-right:0cm; mso-para-margin-bottom:8.0pt; mso-para-margin-left:0cm; line-height:107%; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-fareast-language:EN-US;}

Introduction to cancer biology

Textbook: Introduction to Cancer Biology Robin Hesketh isbn: 9781107601482 Cambridge University Press

BIO 103 - Introduction to Human Biology

Normal 0 false false false EN-US X-NONE X-NONE Course Description: This core curriculum course will concentrate on the quantitative aspects of human biology, including biochemistry, cell biology, molecular physiology and genetics. Emphasis will be placed on molecular mechanisms of cellular processes - such as signal transduction, differential gene expression or self-recognition - that underlie and control pivotal physiological functions of the human organism. Contested topics of modern biology will be introduced and  exmined using scientific method.   Course Learning objectives: Upon successful completion of the course, students should achieve a sound understanding of core concepts of biology and knowledge about the role of various biological macromolecules in the human body, how different types of cells are integrated into multicellular systems, and how organs and organisms develop and function. They will also learn how to apply the scientific method to analysis of various phenomena.   Textbooks and On-Line Materials:   Human Biology 7th Edition by D.D. Chiras, Jones & Bartlett Learning, 2012            ISBN: 9780763783457; ISBN-13:  9780763783457 Textbook companion website: http://biology.jbpub.com/chiras/7e/ Normal 0 false false false EN-US X-NONE X-NONE Semester Schedule: The schedule is subject to change according to the need of the class and the instructor, as determined by the instructor. 1.       September 01 Introduction 2.       September 03 Chapter 1. Course Introductoin; Llife in balance 3.       September 08  Chapter 2. The Chemistry of Life 4.       September 10   Chapter 3 The Life of the Cell 5.       September 15     Chapter 4. Principles of Structure and Function 6.       September 17    Chapter 5. Nutrition and Digestion 7.       September 22    Chapter 5. Nutrition and Digestion (continued) 8.       September 24     Chapter 6. The Circulatory System 9.       September 29      Chapter 7. The Blood 10.    October 01      Chapter 8. The Vital Exchange: Respiration 11.    October 06      Chapter 9. The Urinary System 12.    October 8       Midterm Examination I 13.    October 11 – October 21 Eid Al Adha holidays 14.    October 22      Chapter 10. The Nervous System 15.    October 27      Chapter 11. The Senses 16.    October 29      Chapter 12. The Skeleton and Muscles 17.    November 3    Chapter 13. The Endocrine System 18.    November 5    Chapter 14. The Immune System 19.    November 10  Chapter 15. Human Infectious Diseases 20.    November 12  Chapter 16. Chromosomes, Cell Division, & the Cell Cycle 21.    November 17  Chapter 17. Principles of Human Heredity 22.    November 19  Chapter 17. Principles of Human Heredity, continued 23.    November 24  Midterm Examination II 24.    November 26  Chapter 18. How Genes Are Controlled 25.    December 1    Chapter 19. Genetic Engineering and Biotechnology 26.    December 3    Chapter 20. Cancer 27.    December 8    Chapter 20. Cancer (continued) 28.    December 10  Chapter 21. Human Reproduction 29.    December 15  Chapter 22. Human Development and Aging 30.    December 17 Chapter 23. Evolution 31.    December 22  Chapter 24. Ecology and the Environment 32.    December 24      Midterm Examination III