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Article: Two temporal phases for the control of histone gene activity in cleaving sea urchin embryos (S. purpuratus).

Goustin, A S

1981 Volume 87, Issue 1, Page(s) 163–175

MeSH term(s)	Animals ; Cell Division ; Embryo, Nonmammalian/metabolism ; Female ; Fertilization ; Genes ; Histones/genetics ; Kinetics ; RNA, Messenger/genetics ; Sea Urchins
Chemical Substances	Histones ; RNA, Messenger
Language	English
Publishing date	1981-10-15
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	1114-9
ISSN	1095-564X ; 0012-1606
ISSN (online)	1095-564X
ISSN	0012-1606
DOI	10.1016/0012-1606(81)90069-5
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Article: A Long Non-coding RNA,

Manning, Alisa K / Goustin, Anton Scott / Kleinbrink, Erica L / Thepsuwan, Pattaraporn / Cai, Juan / Ju, Donghong / Leong, Aaron / Udler, Miriam S / Brown, James Bentley / Goodarzi, Mark O / Rotter, Jerome I / Sladek, Robert / Meigs, James B / Lipovich, Leonard

Frontiers in genetics

2020 Volume 11, Page(s) 615

Abstract: Aims: Causal transcripts at genomic loci associated with type 2 diabetes (T2D) are mostly unknown. The chr8p23.1 variant rs4841132, associated with an insulin-resistant diabetes risk phenotype, lies in the second exon of a long non-coding RNA (lncRNA) ... ...

Abstract	Aims: Causal transcripts at genomic loci associated with type 2 diabetes (T2D) are mostly unknown. The chr8p23.1 variant rs4841132, associated with an insulin-resistant diabetes risk phenotype, lies in the second exon of a long non-coding RNA (lncRNA) gene, Methods: We tested our hypothesis using Stellaris fluorescent Results: We found that siRNA knockdown decreased Conclusion: We show that the lncRNA
Language	English
Publishing date	2020-07-10
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2606823-0
ISSN	1664-8021
ISSN	1664-8021
DOI	10.3389/fgene.2020.00615
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Article: Sequence of chemokine receptor gene CCR5 in chimpanzees, a natural HIV type 1 host.

Zacharova, V / Zachar, V / Goustin, A S

AIDS research and human retroviruses

1997 Volume 13, Issue 13, Page(s) 1159–1161

MeSH term(s)	Amino Acid Sequence ; Animals ; CD4 Antigens/genetics ; HIV Infections ; HIV-1/pathogenicity ; Molecular Sequence Data ; Pan troglodytes/genetics ; Phylogeny ; Polymerase Chain Reaction ; Receptors, CCR5/genetics ; Sequence Alignment ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid ; Species Specificity
Chemical Substances	CD4 Antigens ; Receptors, CCR5
Language	English
Publishing date	1997-09-01
Publishing country	United States
Document type	Comparative Study ; Journal Article ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	639130-8
ISSN	1931-8405 ; 0889-2229
ISSN (online)	1931-8405
ISSN	0889-2229
DOI	10.1089/aid.1997.13.1159
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Article: Baculoviral expression of a natural inhibitor of the human insulin receptor tyrosine kinase.

Srinivas, P R / Goustin, A S / Grunberger, G

Biochemical and biophysical research communications

1995 Volume 208, Issue 2, Page(s) 879–885

Abstract: We had earlier reported that the human serum alpha 2-HS glycoprotein (1) is a physiological and specific inhibitor of the human insulin receptor tyrosine kinase (IR-TK). We have now expressed this human protein in the baculoviral expression system using ... ...

Abstract	We had earlier reported that the human serum alpha 2-HS glycoprotein (1) is a physiological and specific inhibitor of the human insulin receptor tyrosine kinase (IR-TK). We have now expressed this human protein in the baculoviral expression system using the Sf-9 and High Five insect cells. The protein was optimally expressed at 72 h post infection. alpha 2-HSGbac completely inhibited the insulin-stimulated autophosphorylation and TK activity of partially purified IR preparations. It also abolished insulin-induced DNA synthesis in the H-35 rat hepatoma cell line. The effective concentration of the baculoviral derived alpha 2-HSG necessary for inhibiting IR-TK activity was significantly lower than that of the protein purified from human plasma.
MeSH term(s)	Animals ; Base Sequence ; Blood Proteins/genetics ; Blood Proteins/pharmacology ; Cell Division/drug effects ; Cloning, Molecular ; DNA Primers/chemistry ; Humans ; In Vitro Techniques ; Insulin/pharmacology ; Molecular Sequence Data ; Nucleopolyhedrovirus ; Phosphorylation ; Protein-Tyrosine Kinases/antagonists & inhibitors ; Receptor, Insulin/antagonists & inhibitors ; Recombinant Proteins/pharmacology ; Spodoptera ; Time Factors ; alpha-2-HS-Glycoprotein
Chemical Substances	AHSG protein, human ; Blood Proteins ; DNA Primers ; Insulin ; Recombinant Proteins ; alpha-2-HS-Glycoprotein ; Protein-Tyrosine Kinases (EC 2.7.10.1) ; Receptor, Insulin (EC 2.7.10.1)
Language	English
Publishing date	1995-03-17
Publishing country	United States
Document type	Journal Article ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	205723-2
ISSN	0006-291X ; 0006-291X
ISSN (online)	0006-291X
ISSN	0006-291X
DOI	10.1006/bbrc.1995.1417
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Article: Absolute quantification of target DNA: a simple competitive PCR for efficient analysis of multiple samples.

Zachar, V / Thomas, R A / Goustin, A S

Nucleic acids research

1993 Volume 21, Issue 8, Page(s) 2017–2018

MeSH term(s)	DNA/analysis ; HIV-1/genetics ; Polymerase Chain Reaction/methods ; Repetitive Sequences, Nucleic Acid
Chemical Substances	DNA (9007-49-2)
Language	English
Publishing date	1993-04-25
Publishing country	England
Document type	Journal Article ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	186809-3
ISSN	0305-1048 ; 0301-5610
ISSN	0305-1048 ; 0301-5610
DOI	10.1093/nar/21.8.2017
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Article ; Online: Reactivation of p53 by novel MDM2 inhibitors: implications for pancreatic cancer therapy.

Azmi, Asfar S / Philip, Philip A / Aboukameel, A / Wang, Zhiwei / Banerjee, Sanjeev / Zafar, Syed F / Goustin, Anton-Scott / Almhanna, K / Yang, Dajun / Sarkar, Fazlul H / Mohammad, Ramzi M

Current cancer drug targets

2010 Volume 10, Issue 3, Page(s) 319–331

Abstract: The present study is the first to show in pancreatic cancer (PC) the growth inhibition and apoptosis by novel MDM2 inhibitors (MI-319 & 219) through reactivation of p53 pathway. Our results highlight two new secondary targets of MDM2 inhibitor 'SIRT1' ... ...

Abstract	The present study is the first to show in pancreatic cancer (PC) the growth inhibition and apoptosis by novel MDM2 inhibitors (MI-319 & 219) through reactivation of p53 pathway. Our results highlight two new secondary targets of MDM2 inhibitor 'SIRT1' and Ku70. SIRT1 which has a role in ageing and cancer and is known to regulate p53 signaling through acetylation. Ku70 is a key component of non-homologous end joining machinery in the DNA damage pathway and is known to regulate apoptosis by blocking Bax entry into mitochondria. Growth inhibition and apoptosis by MI-219, MI-319 was accompanied by increase in levels of p53 along with p21(WAF1) and the proapoptotic Puma. SiRNA against p21(WAF1) abrogated the growth inhibition of PC cells confirming p21(WAF1) as a key player downstream of activated p53. Immunoprecipitation-western blot analysis revealed reduced association of MDM2-p53 interaction in drug exposed PC cells. In combination studies, the inhibitors synergistically augmented anti-tumor effects of therapeutic drug gemcitabine both in terms of cell growth inhibition as well as apoptosis. Surface plasmon resonance studies confirmed strong binding between MI-319 and Ku70 (K(D) 170 nM). Western blot revealed suppression of SIRT1 and Ku70 with simultaneous upregulation of acetyl-p53 (Lys379) and Bax. Co-Immunoprecipitation studies confirmed that MI-319 could disrupt Ku70-Bax and SIRT1-Bax interaction. Further, using wt-p53 xenograft of Capan-2, we found that oral administration of MI-319 at 300 mg/kg for 14 days resulted in significant tumor growth inhibition without any observed toxicity to the animals. No tumor inhibition was found in mut-p53 BxPC-3 xenografts. In light of our results, the inhibitors of MDM2 warrant clinical investigation as new agents for PC treatment.
MeSH term(s)	Animals ; Antigens, Nuclear/metabolism ; Antineoplastic Agents/pharmacology ; Apoptosis/drug effects ; Blotting, Western ; Cell Cycle/drug effects ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Cyclin-Dependent Kinase Inhibitor p21/metabolism ; DNA-Binding Proteins/metabolism ; Deoxycytidine/analogs & derivatives ; Deoxycytidine/pharmacology ; Dose-Response Relationship, Drug ; Enzyme Inhibitors/pharmacology ; Female ; Humans ; Immunoprecipitation ; Indoles/pharmacology ; Ku Autoantigen ; Mice ; Mice, Inbred ICR ; Mice, SCID ; Pancreatic Neoplasms/drug therapy ; Pancreatic Neoplasms/enzymology ; Pancreatic Neoplasms/genetics ; Pancreatic Neoplasms/pathology ; Protein Binding ; Proto-Oncogene Proteins c-mdm2/antagonists & inhibitors ; Proto-Oncogene Proteins c-mdm2/metabolism ; RNA Interference ; Sirtuin 1/metabolism ; Spiro Compounds/pharmacology ; Surface Plasmon Resonance ; Time Factors ; Transfection ; Tumor Burden ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism ; Xenograft Model Antitumor Assays ; bcl-2-Associated X Protein/metabolism
Chemical Substances	Antigens, Nuclear ; Antineoplastic Agents ; BAX protein, human ; CDKN1A protein, human ; Cyclin-Dependent Kinase Inhibitor p21 ; DNA-Binding Proteins ; Enzyme Inhibitors ; Indoles ; MI 319 ; MI-291 ; Spiro Compounds ; TP53 protein, human ; Tumor Suppressor Protein p53 ; bcl-2-Associated X Protein ; Deoxycytidine (0W860991D6) ; gemcitabine (B76N6SBZ8R) ; MDM2 protein, human (EC 2.3.2.27) ; Proto-Oncogene Proteins c-mdm2 (EC 2.3.2.27) ; SIRT1 protein, human (EC 3.5.1.-) ; Sirtuin 1 (EC 3.5.1.-) ; Xrcc6 protein, human (EC 3.6.4.12) ; Xrcc6 protein, mouse (EC 3.6.4.12) ; Ku Autoantigen (EC 4.2.99.-)
Language	English
Publishing date	2010-04-07
Publishing country	Netherlands
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	2064824-8
ISSN	1873-5576 ; 1568-0096
ISSN (online)	1873-5576
ISSN	1568-0096
DOI	10.2174/156800910791190229
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Article: Direct measurement of histone peptide elongation rate in cleaving sea urchin embryos.

Goustin, A S / Wilt, F H

Biochimica et biophysica acta

1982 Volume 699, Issue 1, Page(s) 22–27

Abstract: ... indicate an elongation rate (at 15 degrees C) for histones H2B and H1 alpha of 0.69 and 0.80 codons per s ...

Abstract	Regulation of protein synthesis can be exercised at a number of levels. One of the more experimentally difficult levels to approach has been the measurement of peptide elongation rate. This paper presents a new application of the cyanogen bromide (CNBr) cleavage of proteins in a direct measurement of histone peptide elongation rate in cleaving sea urchin embryos (Strongylocentrotus purpuratus). The data indicate an elongation rate (at 15 degrees C) for histones H2B and H1 alpha of 0.69 and 0.80 codons per s, respectively. These values fall within the range of previously published values of average peptide elongation rate for total protein in these cells. This method should be generally applicable to many systems for which the measurement of peptide elongation rate may provide a key to the understanding of the regulation of protein synthesis.
MeSH term(s)	Animals ; Cell Division ; Embryo, Nonmammalian/physiology ; Female ; Histones/genetics ; Kinetics ; Peptide Chain Elongation, Translational ; Peptide Fragments/analysis ; Sea Urchins
Chemical Substances	Histones ; Peptide Fragments
Language	English
Publishing date	1982-10-29
Publishing country	Netherlands
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	60-7
ISSN	1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
ISSN (online)	1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650
ISSN	0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
DOI	10.1016/0167-4781(82)90167-1
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Article: Protein synthesis, polyribosomes, and peptide elongation in early development of Strongylocentrotus purpuratus.

Goustin, A S / Wilt, F H

Developmental biology

1981 Volume 82, Issue 1, Page(s) 32–40

MeSH term(s)	Animals ; Blastocyst/metabolism ; Embryo, Nonmammalian/metabolism ; Female ; Fertilization ; Kinetics ; Ovum/metabolism ; Peptide Chain Elongation, Translational ; Polyribosomes/metabolism ; Protein Biosynthesis ; Sea Urchins/metabolism
Language	English
Publishing date	1981-02
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID	1114-9
ISSN	1095-564X ; 0012-1606
ISSN (online)	1095-564X
ISSN	0012-1606
DOI	10.1016/0012-1606(81)90426-7
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Article: Sheep red blood cells armed with anti-CD20 single-chain variable fragments (scFvs) fused to a glycosylphosphatidylinositol (GPI) anchor: a strategy to target CD20-positive tumor cells.

Hamdy, Nayera / Goustin, Anton Scott / Desaulniers, Jean-Paul / Li, Mei / Chow, Christine S / Al-Katib, Ayad

Journal of immunological methods

2005 Volume 297, Issue 1-2, Page(s) 109–124

Abstract: Single-chain variable fragment antibodies (scFv) retain antigen specificity and offer advantages over intact antibodies as therapeutic agents. We cloned the cDNA of the V(H) and V(kappa) regions from a mouse hybridoma (HB-9645) directed against human ... ...

Abstract	Single-chain variable fragment antibodies (scFv) retain antigen specificity and offer advantages over intact antibodies as therapeutic agents. We cloned the cDNA of the V(H) and V(kappa) regions from a mouse hybridoma (HB-9645) directed against human CD20. In addition to the basic scFv construct (V(kappa)-L-V(H)), we genetically engineered a secretory signal, six histidine residues, and a 'Flu' tag to facilitate secretion, purification, and detection. A glycosyl-phosphatidylinositol (GPI) modification signal was added at the C terminus. The GPI-tagged and the non-tagged scFvs were expressed in high yields on the surface of stably transfected insect cells. The CD20-binding properties of purified non-GPI tagged scFv were examined using flow cytometry and immunocytochemistry. The non-GPI-tagged scFv selectively recognizes CD20-positive cells in a concentration-dependent manner. Double-flow cytometry analysis using fresh peripheral blood lymphocytes and WSU-FSCCL cells revealed that our scFv resolves the B-cell population better than the intact antibody. The GPI-tagged scFv was loaded onto the surface of sheep erythrocytes to form rosettes with CD20-positive cells. The genetically engineered anti-CD20 scFv and GPI-tagged derivative have binding specificity for the CD20 antigen. The scFvs described here has potential uses as an in vivo tumor-imaging agent and as a carrier vehicle for targeted delivery of cytocidal agents to CD20-positive cancer cells.
MeSH term(s)	Amino Acid Sequence ; Animals ; Antigens, CD20/analysis ; Antigens, CD20/immunology ; Antigens, Neoplasm/analysis ; Antigens, Neoplasm/immunology ; Base Sequence ; Cloning, Molecular ; Erythrocytes/immunology ; Glycosylphosphatidylinositols/genetics ; Humans ; Immunoglobulin Variable Region/genetics ; Immunoglobulin Variable Region/immunology ; Immunoglobulin Variable Region/therapeutic use ; Mice ; Molecular Sequence Data ; Neoplasms/therapy ; Recombinant Fusion Proteins/genetics ; Recombinant Fusion Proteins/immunology ; Rosette Formation ; Sheep
Chemical Substances	Antigens, CD20 ; Antigens, Neoplasm ; Glycosylphosphatidylinositols ; Immunoglobulin Variable Region ; Recombinant Fusion Proteins
Language	English
Publishing date	2005-02
Publishing country	Netherlands
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	120142-6
ISSN	1872-7905 ; 0022-1759
ISSN (online)	1872-7905
ISSN	0022-1759
DOI	10.1016/j.jim.2004.12.003
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Article: Platelet-derived growth factor and its receptor in blood cell differentiation and neoplasia.

Pantazis, P / Goustin, A S / Nixon, J

European journal of haematology

1990 Volume 45, Issue 3, Page(s) 127–138

Abstract: Platelet-derived growth factor (PDGF) is a family of dimeric protein molecules synthesized by differentiated, non-dividing and proliferating blood cells. Experimental findings indicate that PDGF is involved in development and/or maintenance of ... ...

Abstract	Platelet-derived growth factor (PDGF) is a family of dimeric protein molecules synthesized by differentiated, non-dividing and proliferating blood cells. Experimental findings indicate that PDGF is involved in development and/or maintenance of physiological functions of certain normal blood cells. Also, PDGF synthesis correlates with certain blood cell proliferative diseases caused either spontaneously or associated with viral infection. There is increasing evidence that the diverse effects of PDGF in both normal and abnormal physiological functions of blood cells may be regulated at the level of its receptor. New experimental findings are discussed relating to PDGF receptors in normal leukemic, and virally-infected human cells of myeloid and lymphocytic lineages. At specific developmental stages this regulation may take the form of PDGF and its receptor being expressed or co-expressed; the unmodified or modified form of receptor that specifically interacts with PDGF; the cellular site at which the PDGF-receptor interacts with its ligand; and co-expression of the PDGF-receptor with other receptors associated with specific cell lineage or functions. Elucidation of events involved in synthesis, processing, and interactions of PDGF isoforms and their respective receptors will enable us to develop pharmacological means that may either interfere with, or enhance these desired blood cell functions. This review focuses on PDGF and its receptor in human blood cell differentiation and neoplasia.
MeSH term(s)	Blood Cells/pathology ; Cell Differentiation ; Deltaretrovirus/physiology ; Humans ; Leukemia/pathology ; Platelet-Derived Growth Factor/genetics ; Platelet-Derived Growth Factor/physiology ; RNA, Messenger/metabolism ; Receptors, Cell Surface/physiology ; Receptors, Platelet-Derived Growth Factor ; T-Lymphocytes/metabolism ; T-Lymphocytes/microbiology ; T-Lymphocytes/pathology
Chemical Substances	Platelet-Derived Growth Factor ; RNA, Messenger ; Receptors, Cell Surface ; Receptors, Platelet-Derived Growth Factor (EC 2.7.10.1)
Language	English
Publishing date	1990-09
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Review
ZDB-ID	392482-8
ISSN	1600-0609 ; 0902-4441
ISSN (online)	1600-0609
ISSN	0902-4441
DOI	10.1111/j.1600-0609.1990.tb00439.x
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