Tulane Cancer Center Members: S
Faculty Membership Application and
Membership Definitions
A B C D E
F G H I J
K L M N
O
P Q R S
T U V W X
Y Z
Safah, Sanford, Santos, Scandurro, Schally, Scher, Schorin, Sikka, Srivastav, Steinmann, Stolier, Sullivan
Hana Safah, M.D.
Director of Bone Marrow Transplant
Associate Professor of Medicine
Section of
Hematology and Medical Oncology
TCC Associate Member
hsafah@tulane.edu
(504) 599-6565, (504) 988-6077 fax
1430 Tulane Ave., Box SL-68, New Orleans, LA 70112-2699
Specialties, publications, and research:
- Lymphoma, leukemia, bone marrow transplant, clinical research
- "Chronic myelogenous leukemia protocol" (Schering)
- "Efficacy and safety of PEG-rHuMGDF in patients with delayed
platelet engraftment" (Amgen)
- Safah H,
Weiner RS
"The role of bone marrow transplantation in the management of advanced
local disease"
Robert Sanford, Ph.D.
Radiation Oncologist
Assistant Professor of Radiology
TCC Associate Member
rsanford@tulane.edu
(504) 988-6314, (504) 988-6362 fax
1415 Tulane Ave., Box HC-62, New Orleans, LA 70112
Biographical information:
Dr. Sanford received his B.S. in Mechanical
Engineering in 1984 from Tulane University with one year of study
at the University of Sheffield,
England. He received his Masters and Ph.D. degrees in Particle Physics
in 1999 from Louisiana State University.
Dr. Sanford began a medical physics residency in 1999 under Dr. M.S.
Al-Ghazi at the University of
California, Irvine and was bestowed a Young Physicist Award by the American College of Medical Physics in
2000. Dr. Sanford continued at UCI as a clinical instructor and joined
the Tulane faculty in February 2002.
Dr. Sanford's primary clinical duties include the calibration, quality
assurance, acceptance testing, and commissioning of all radiation
therapy equipment, radioactive treatment sources, computerized
treatment planning systems, and radiation measuring devices housed in
the Department of Radiation Oncology.
Clinical responsibilities also include overseeing the determination of
radiation dose distributions in patients undergoing treatment and
tracking doses delivered to patients. Research interests include
intensity modulated radiation therapy (IMRT) and Monte Carlo treatment
planning.
Recent Publications:
-
Sanford R. (1999) Observation of the
east-west anisotrophy of the atmospheric neutrino flux. Phys Rev Lett 82: 5194-5197.
- Sanford R. (1999) Measurement of
the solar neutrino energy spectrum using neutrino-electron scattering. Phys Rev Lett 82: 2430-2434.
- Sanford R. (1999) Constraints on
neutrino oscillation parameters from the day-night soalr neutrino
fluxes at Super-Kamiokande. Phys Rev
Lett 82: 1810-1814.
- Sanford R. (2000) Tan neutrinos
favored over sterile neutrinos in atmospheric muon neutrinos in
atmospheric muon neutrino oscillations. Phys Rev Lett 83: 3999-4003.
Edgardo S. Santos, M.D.
Assistant Medical Director, Office of
Clinical Research
Assistant Professor of Medicine
Section of
Hematology and Medical Oncology
TCC Contributing Member
esantos1@tulane.edu
(504) 988-6352, (504) 988-5483 fax
1430 Tulane Ave., Box SL-78, New Orleans, LA 70112-2699
Biographical information:
Dr. Santos received his medical degree in 1994 at the University of
Panama School of Medicine, Panama. He completed his internship years at
Complejo Hospitalario Metropolitano "Dr. Anulfo Arias Madrid", Panama
(1994-1995) and Hospital Regional de Santiago, Veraguas (1995-1996). He
was ranked first for the Internal Medicine residency program at
Complejo Hospitalario Metropolitano (1997). Dr. Santos continued and
finished his training in Internal Medicine at Jackson Memorial
Hospital, University of Miami,
Florida (1998-2001). During his fellowship (2001-2004), Dr. Santos
participated actively in the development of several clinical and
translational research projects at Sylvester
Comprehensive Cancer Center, Miami, Florida. His major interest has
been the development of Phase I and Phase II clinical trials for
hematologic malignancies such as multiple myeloma and lymphoma. Dr.
Santos has also been involved in several clinical projects focusing on
lung cancer. He joined the Tulane University faculty as Assistant
Professor of Medicine, in the section of Hematology and Medical
Oncology (2004). He also serves as Physician Staff at the Veterans Affairs Medical Center, New
Orleans. He has the responsibility to supervise the Hematology-Oncology
outpatient facility, the Chemotherapy Unit, and the in-patient service.
In addition to his patient care activities at the V.A. Hospital and at Tulane Cancer Center, Dr. Santos is
involved with the training of medical students, residents, and fellows.
He is an active member of sereval medical societies such as the American Society of Hematology, the American Society of Clinical Oncology,
the American Association for Cancer
Research, the American College of
Physicians-American Society of Internal Medicine. Dr. Santos
was recipient of the "Spirit Award" from the American Cancer Society in
the summer of 2005 and was named assistant medical director of Tulane
Cancer Center's Office of Clinical Research in August 2005.
Recent Publications:
- Santos, E. Lung Cancer Vaccines. In Cancer Vaccine: New Research,
Nova Science Publishers, 2006.
- Raez LE, Santos ES, Mudad R, Podack ER. Clinical trials
targeting lung cancer with active immunotherapy: the scope of
vaccines. Expert Rev
Anticancer Ther, 5(4): 635-644, 2005.
- Santos ES, Raez LE, DeCesare T, Singal R. DNA methylation:
its role in lung carcinogenesis and therapeutic implications. Expert Rev Anticancer Ther, 5(4):
667-679, 2005.
- Santos ES, Masri M, Safah H. Revisiting the role of
hematopoietic stem cell transplantation in chronic lymphocytic
leukemia. Expert Rev
Anticancer Ther, 5(4): 875-891, 2005.
- Morgensztern D, Rosado M, Raez L, Santos ES,
Cassileth P. Combination of imatinib and cytarabine for the treatment
of Philadelphia chromosome positive acute lymphoblastic leukemia. Leuk Lymphoma 46(2):297-8. (Feb.
2005)
- Morgensztern D, Rosado M, Silva O, Santos
ES, Abdullah S, Goodman M, Hamilton-Nelson K, Rosenblatt J,
Lossos I. Prevalence of hepatitis C infection in patients with
non-Hodgkin's lymphoma in South Florida and review of the literature. Leuk Lymphoma 45(12):2459-64. (Dec.
2004)
- Santos ES, Raez LE, Eckardt P,
DeCesare T, Whitcomb CC, Byrne GE Jr. The utility of a bone marrow
biopsy in diagnosing the source of fever of unknown origin in patients
with AIDS. J AIDS 37(5):
1599-1603 (2004)
- Santos ES, Rosenblatt JD, Goodman
M. The role of farnesyltransferase inhibitors in hematologic
malignancies. Expert Rev Anticancer
Ther 4(5):834-856 (2004
- Raez LE, Rosado MF, Santos ES,
Reis IM. Irontecan and Docetaxel as first-line chemotherapy in patients
with stage IIIB/IV non-small-cell lung cancer: experience from a
prematurely closed Phase II study. Lung
Cancer 45:131-132 (2004)
- Santos ES, Goodman, Byrnes JJ,
Fernandez HF. Thalidomide effects in the post-transplantation setting
in patients with multiple myeloma. Hematology
9:35-39 (2004)
- Santos ES, Raez LE, Salvatierra J,
Morgensztern D, Shanmugan N, Neff GW. Primary hepatic non-Hodgkin
lymphomas: a review of literature.
Am J Gastroenterol
98:2789-2793 (2003)
- Santos ES, Rosenblatt JD. Combining
interleukin-2 with monoclonal antibody therapy for treatment of
non-Hodgkin's lymphomas. Immune-Enhancing
Cytokines 5:7-10 (2003)
- Jy W, Gagliano-DeCesare T, Kett DH, Horstman LL, Jimenez JJ,
Ruiz-Dayao Z, Santos ES, Ahn YS.
Life-threatening bleeding from refractory acquired FVIII inhibitor
successfully treated with Rituximab. Acta
Haematol 109:206-208 (2003)
- Santos ES, Raez LE, Kharfan-Dabaja
MA, Angulo J, Restrepo A, Byrnes JJ. Renal allograft survival in de
novo hemolytic uremic syndrome (HUS) after kidney transplantation. Transplant Proc 35:1370-1374 (2003)
- Kharfan-Dabaja MA, Morgensztern D, Santos
ES, Goodman M, Fernandez HF. Acute graft-versus-host disease
(aGVHD) presenting with an acquired lupus anti-coagulant.
Bone Marrow Transplant
31:129-131 (2003)
Aline B. Scandurro, Ph.D.
Research Assistant Professor of Microbiology
TCC Program Member
alibscan@tulane.edu
(504) 988-1934, (504) 988-5144 fax
1601 Perdido Street, New Orleans, LA 70112
Homepage on the Microbiology website:
http://www.som.tulane.edu/departments/microbiology/scandurro.htm
Biographical information:
Dr. Scandurro received her B.S. in Biochemistry from Tulane
University in 1985. She received her Ph.D. in 1992 in Microbiology from
Georgetown University Medical
Center and completed a postdoctoral fellowship in 1993 at the National Institutes of Health,
Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute. She
completed a second fellowship in 1997 at the Tulane
Cancer Center, Department of
Pharmacology, Tulane University Medical Center, She joined the
Tulane faculty in 1997 as a Research Instructor and became a Research
Assistant Professor in 1999.
Dr. Scandurro's research focuses on oxygen-sensing genetic mechanisms,
post-transcriptional control of oxygen-regulated genes, RNA binding
proteins, angiogenesis and cancer research. Tumors require the
formation of new blood vessels, angiogenesis, to grow. Targeting
angiogenesis provides a novel approach for cancer therapy that rivals
conventional therapy since drug resistance and tissue toxicity issues
are avoided. Tumor angiogenesis depends on a balance between
tumor-dependent angiogenic factors like VEGF (vascular endothelial
growth factor) and host anti-angiogenic peptides like endostatin and
angiostatin. The ability to alter this balance by favoring the
anti-angiogenic effect by treatment with exogenous endostatin and
angiostatin has been demonstrated. However, a major difficulty in
translating these strategies to the clinic is the lack of large
quantities of these peptides for long-term treatment. An alternative
strategy to disturb this balance is to disrupt VEGF or other angiogenic
factor production. EGF, like the hematopoietic growth factor
erythropoietin (Epo), is usually synthesized following low oxygen or
hypoxic stress. Since VEGF is a potent mitogen for vascular endothelial
cells this response represents a means to quickly develop new blood
vessels to bring oxygenated red blood cells and rescue the stressed
tissue. Growing tumor cells become hypoxic and trigger or exploit this
normal physiologic process. VEGF and Epo induction by hypoxia is
largely controlled at the level of message stability.
Post-transcriptional mechanisms have been implicated for VEGF and Epo
since a physiologic drop in oxygen tension leads to induction of gene
expression. However, increases in mRNA transcription does not exactly
parallel the observed increased level of expression; thus it has been
postulated that post-transcriptional stabilization of the normally
labile VEGF and Epo mRNAs may account for the observed increased VEGF
and Epo levels. Investigations in this laboratory have identified a
complex of proteins, erythropoietin mRNA binding protein complex
(ERBP30 and 70), in cytoplasmic lysates of human hepatocellular
carcinoma (Hep3B) cells which specifically bind to a 120 nucleotide
(nt) region in the 3' untranslated region (UTR) of Epo mRNA, VEGF mRNA
as well as tyrosine hydroxylase (TH) mRNA. Additionally, a stabilizing
role has been suggested for this region from studies in which deletion
of this 120 nt region lead to an unchanged mRNA half-life in response
to hypoxia (6 hrs) as compared to a forty percent increase in half-life
observed for the wild-type mRNA. Production of VEGF and Epo is likely
to be controlled post-transcriptionally by specific binding of the
ERBP30 and ERBP70 complex to the 3' UTR of the VEGF and Epo mRNA.
Current efforts are centered on understanding oxygen-sensing at the
post-transcriptional level with the hypothesis that ERBP30 and ERBP70
are common post-transcriptional factors involved in oxygen-sensing.
Recent Publications:
-
Scandurro AB, McGary E, Rondon IJ,
Wilson R, Beckman BS. (1995) Redox
and heat shock protein HSP70 affect the binding of erythropoietin RNA
binding protein to erythropoietin mRNA. Acta Hematologica 93: 216.
- Scandurro AB, Rondon IJ, Wilson
RB, Tennenbaum SA, Garry RF, Beckman BS. (1997) Interaction of
erythropoietin RNA binding protein with mRNA requires an association
with heat shock protein 70. Kidney Int
51(2): 579-584.
- Mallia CM, Aguirre V, McGary E, Tang Y, Scandurro
AB, Liu C, Noguchi CT, Beckman BS.
(1998) Protein kinase C is an effector of hexamethylene
bisacetamide-induced differentiation of friend erythroleukemia cells. Exp Cell Res 246: 348-354.
- Scandurro AB, Beckman BS. (1998) Common Proteins bind
mRNAs encoding Erythropoietin, Tyrosine Hydroxylase and Vascular
Endothelial Growth Factor. Biochem
Biophys Res Comm 246: 436-440.
- Ohigashi T, Mallia CS, McGary E, Scandurro
AB, Rondon IJ, Fisher JW, Beckman BS. (1999) Protein kinase C
alpha protein expression is necessary for sustained erythropoietin
production in human hepatocellular carcinoma (Hep3B) cells exposed to
hypoxia. Biochim Biophys Acta
1450(2): 109-18.
- Godin DA, Fitzpatrick PC, Scandurro AB,
Belafsky PC, Woodworth BA. Amedee
RG, Beech DJ, Beckman BS. (2000)
PH20: a novel tumor marker for laryngeal cancer. Arch Otolaryngol Head Neck Surg
126(3): 402-4.
-
Additional publications and abstracts
Andrew V. Schally, Ph.D.
Professor of Medicine
Experimental Medicine,
Veterans Administration Hospital
TCC Program Member
(504) 589-5230, (504) 566-1625 fax
1601 Perdido Street, New Orleans, LA 70112
Biographical information:
Dr. Schally's research career began in December 1949 at the National Institute for Medical
Research (Mill Hill), London, England, where he was trained in
peptide chemistry. Between 1952 and 1957 he studied biochemistry and
Endocrinology at McGill University,
Montreal, Canada and worked in the Endocrine unit at Allan Memorial
Institute for Psychiatry. In 1957, Dr. Schally moved to Baylor University in Houston, Texas
to work on corticotropin-releasing factor (CRF). In 1962 he joined the Veterans Administration Hospital and the
Department of Medicine at Tulane
University School of Medicine in New Orleans. Dr. Schally
outstanding research accomplishments were recognized in 1977 when he
was awarded the Nobel Prize in Medicine for his work on the isolation,
identification, synthesis and clinical application of hypothalamic
hormones. Currently Dr. Schally is studying the development of new
cancer therapies based on antitumor peptides. The long-term objective
of this research is the development of new hormonal methods for
treatment of various neoplasms, which may be dependent on or sensitive
to hormones and growth factors. The specific aims are to evaluate
antitumor activity of some peptide analogs of hypothalmic hormones,
especially antagonists of leutinizing hormone releasing hormone
(LH-RH), antagonists of growth hormone releasing hormone (GH-RH),
antagonists of bombesin/gastrin releasing peptide (GRP), cytotoxic
analogs of LH-RH, somatostatin and bombesin, and to elucidate the
mechanism of action of these analogs. This includes evaluation of
changes in the expression of growth factors and their membrane
receptors by measurements of mRNA levels in tumors. The inhibitory
effects of analogs are studied in various animal tumor models,
especially in nude mice bearing transplanted human cancers. The
antitumor action of analogs is due to various effects on hormones,
growth factors, or their receptors. The overall program provides new
information on the application of peptide analogs for treatment of
neoplasms for which present therapy is inadequate, such as relapsed
androgen-independent prostate cancer, advanced pancreatic cancer,
locally-advanced and metastatic gastric cancer, disseminated colon
cancer, malignant brain tumora, lung cancer (SCLC and non-SCLC), renal
cancer and tumors of bone and cartilage.
Recent Publications:
-
Rekasi Z, Czompoly, Schally AV,
Halmos G. (2000) Isolation and sequencing of cDNAs for splice variants
of growth hormone-releasing hormone receptors from human cancers. Proc Natl Acad Sci USA 97(19):
10561-10566.
- Andrew V. Schally, Ph.D., Ana Maria Comaru-Schally, M.D.. (2000)
"Hypothalamic and Other Peptide Hormones". Eds: James F. Holland, Emil
Frei III, Robert C. Bast Jr., Donald W. Kufe, Raphael E. Pollock and
Ralph R. Weichselbaum. B.C. Dekker Publishers, Ontario. Cancer
Medicine 5th edition, Ch 53: 715-729.
- Chatzistamou, I., Schally AV,
Varga JL, Groot K, Armatis P, Busto R, Halmos G. (2001) Antagonists of
growth hormone-releasing hormone and somatostatin analog RC-160 inhibit
the growth of the OV-1063 human epithelial ovarian ca. cell line
xenografted into nude mice. J Clin
Endocrinol Metab 86(5): 2144-2152.
- Kovacs, M., Schally AV,
Csernus B, Rekasi Z. (2001) Leutinizing hormone-releasing (LH-RH)
antagonist Cetrorelix down-regulates the mRNA expression of pituitary
receptors for LHRH by counteracting the stimulatory effect of
endogenous LHRH. Proc Natl Acad Sci
USA 98: 1829-1834.
- Rekasi, Z., J.L. Varga, Schally AV,
Plonowski A, Halmos G, Csernus B, Armatis P, Groot K. (2001)
Antiproliferative actions of Growth Hormone-Releasing Hormone (GHRH)
antagonists on MiaPaCa-2 human pancreatic cancer cells involve cAMP
independent pathways. Peptides
22: 879-886.
- Nagy A, Schally AV. (2001)
Targeted cytotoxic somatostatin analogs : A modern approach to the
therapy of various cancers. Drugs of
the Future 98: 1829-1834.
Charles D. Scher, M.D.
Marcelle Shaeffer Vergara Chair Professor of Pediatrics
Chief of the Section of Pediatric
Hematology-Oncology
TCC Associate Member
cscher@tulane.edu
(504) 988-5412, (504) 988-2557 fax
1430 Tulane Ave., Box SL-37, New Orleans, LA 70112-2699
Biographical information:
Dr. Scher received his B.A. in 1961 from Brandeis University and earned his
medical degree in 1965 from the University
of Pennsylvania. He served an internship and residency at Bronx
Municipal Hospital/Albert Einstein
College of Medicine in New York and a residency in pediatrics
fellowship in pediatric hematology at Children's Hospital Medical
Center, Harvard Medical
School. He also served as a lieutenant commander from 1967-1971 in
the United States Public Health Service at the National Cancer Institute in
Bethesda, Maryland. After teaching and research fellowships in
pediatrics at Harvard Medical School, Dr. Scher joined the Harvard
faculty where he rose to the rank of associate professor of pediatrics.
While at Harvard he was a visiting scientist in the Department of
Biology at the Massachusetts Institute of
Technology. Dr. Scher joined the University of Pennsylvania Medical
School in 1982 as professor of pediatrics and human genetics. He joined
the Tulane faculty in 1994. Dr. Scher specializes in pediatric hematology and oncology.
He has served as bench researcher, mentor, and reviewer in
investigations in acute lymphoblastic leukemia and the molecular
biology of cancer. Dr. Scher is an accomplished basic scientist in the
fields of the cellular and molecular biology of cancer, especially in
the definition of the viruses causing leukemia, and the study of
platelet derived growth factor, which has been implicated in the
replication of normal connective tissue cells as in process of wound
healing. He has served as principal investigator on six NIH-funded projects and one privately
funded grant project, and has been responsible for extramural funding
for numerous graduate students and junior faculty working in his
laboratories. He is author of over 90 original publications and
abstracts in his field.
Recent Publications:
-
Belasco JB, Luery N, Scher CD. (1990)
Multiagent chemotherapy in relapsed acute lymphoblastic leukemia in
children. Cancer 66: 2492-2497.
- Meister L, Uri A, Agrons G, Scher CD.
(1993) Wilms' tumor bone metastases at diagnosis. Med Ped Oncol 21: 446-450.
- Kahn MJ, Scher
CD, Rozans MR, Michaels RK, Leissinger C, Krause J. (1997) Factor V Leiden is not
responsible for stroke in patients with sickling disorders and is
uncommon in African Americans with sickle cell disease. Am J Hem 54: 12-15.
- Adams RJ, McKie VC, Hsu L, Files B, Vichinsky E, Pegelow C,
Abboud M, Gallagher D, Kutlar A, Nichols FT, Bonds DR, Brambilla D,
Woods G, Olivieri N, Driscoll C, Miller S, Wintred W, Huriett A, Scher CD, Berman B, Carl E, Jones AM, Roach ES,
Wright E, Zimmerman RA, Waclawiw M. (1998) Prevention of a first stroke
by transfusions in children with sickle cell anemia and abnormal
results on transcranial doppler ultrasonography. New Eng J Med 339: 5 - 11.
- Leahey AM, Bunin NJ, Belasco JB, Meek R, Scher
CD, Lange BJ. (2000) Novel multiagent chemotherapy for bone
marrow relapse of pediatric acute lymphoblastic leukemia. Med Ped Oncol 34: 313-318.
Marshall A. Schorin, M.D.
Professor of Pediatrics
Section of Pediatric
Hematology-Oncology
Principle Investigator at Tulane for COG studies
TCC Program Member
mschori@tulane.edu
(504) 988-5412, (504) 988-2557 fax
1430 Tulane Ave., Box SL-37, New Orleans, LA 70112-2699
Biographical information:
Dr. Schorin graduated from the Massachusetts
Institute of Technology and earned an M.D. from the University of Pennsylvania School of
Medicine. After serving at the University of Rochester
School of Medicine and Dentistry and at Harvard Medical School,
he joined the faculty of the Tulane University School of Medicine in
1983. Dr. Schorin is engaged in developing and administering
chemotherapy protocols,
particularly including clinical research in the management of childhood
acute lymphoblastic leukemia, in affiliation with the Dana Farber Cancer Institute,
Boston, Massachusetts. He is also involved in similar research and
treatment of childhood cancer through membership in the Children's
Oncology Group (COG).
He is the Principal Investigator at the Tulane site of the COG and a
member of the steering committee of the Transfusion Medicine/Hemostasis
Ntework established by the National Institutes of Health (NIH).
Recent Publications:
-
Silverman LB, Declerck L, Gelber RD, Dalton VK, Asselin BL, Barr RD,
Clavell LA, Hurwitz CA, Moghrabi A, Samson Y, Schorin
MA, Lipton JM, Cohen HJ, Sallan SE. Results of Dana-Farber
Cancer Institute Consortium protocols for children with newly diagnosed
acute lymphoblastic leukemia (1981-1995). Leukemia 14(12):2247-56 (2000)
- Silverman LB, Gelber RD, Dalton VK, Asselin BL, Barr RD, Clavell
LA, Hurwitz CA, Moghrabi A, Samson Y, Schorin MA,
Arkin S, Declerck L, Cohen HJ, Sallan SE. Improved outcome for children
with acute lymphoblastic leukemia: results of Dana-Farber Consortium
Protocol 91-01. Blood
97(5):1211-8 (2001)
- LeClerc JM, Billett AL, Gelber RD, Dalton V, Tarbell N, Lipton
JM, Barr R, Clavell LA, Asselin B, Hurwitz C, Schorin
MA, Lipshultz SE, Declerck L, Silverman LB, Cohen HJ, Sallan
SE. Treatment of childhood acute lymphoblastic leukemia: Results of
Dana-Farber ALL consortium protocol 87-01. J Clin Oncol 20(1):237-46 (2002)
- Lipshultz SE, Giantris AL, Lipsitz SR, Dalton VK, Asselin BL,
Barr RD, Clavell LA, Hurwitz CA, Moghrabi A, Samson Y, Schorin MA, Gelber RD, Sallan SE, Colan SD.
Doxorubicin administration by continuous infusion is not
cardioprotective: The Dana-Farber 91-01 Acute Lymphoblastic Leukemia
Protocol. J Clin Oncol
20(6):1677-1682 (2002)
Suresh C. Sikka, Ph.D., HCLD
Associate Professor of Urology
Adjunct Associate Professor of
Pharmacology and Biochemistry
Director of
Andrology Clinic and Research Laboratories
TCC Associate Member
ssikka@tulane.edu
(504) 988-5179, (504) 988-5059 fax
1430 Tulane Ave., Box SL-42, New Orleans, LA 70112-2699
Homepage on the Urology website:
http://www.som.tulane.edu/departments/urology/faculty/sikka.html
Biographical information:
Dr. Sikka received his Ph.D. from the Department of Pharmacology, Post
Graduate Institute of Medical Education and Research (PGIMER),
Chandigarh, India, in 1978. He did his post-doctoral fellowship from
1979-1982 in the Department of Biochemistry at the University of
Southern California (USC), Los
Angeles where he obtained training in the field of protein-lipid
interactions in cell membranes, protein purification, and functional
incorporation into liposomes. In 1982 Dr. Sikka moved to the Urology
section of the Department of Surgery at Harbor-UCLA
Medical Center, University of California Los Angeles (UCLA), as
Urology Laboratory Research Director. Dr. Sikka joined the Tulane
faculty in 1989 as Assistant Professor of Urology and Andrology
Laboratory Director. He was responsible for setting up a
CLIA-approved Andrology Clinical and Research Laboratory at Tulane
Medical Center, catering to the needs of many infertility and sexual
dysfunction patients. Dr. Sikka's current research focus is oxidative
stress-related signal transduction pathways and gene expression
involved in prostate tumorigenesis (BPH and cancer) and drug targeting.
The Urology department has recently procured a Laser Capture Microscope
(LCM) to microdissect specific and selective biological cells from
various clinical samples. LEQSF has also recently funded the Department
to acquire the latest DNA - microarray system for expression of
specific genes (genomics), and their translational products
(proteonomics). The lab routinely employs molecular biology,
differential gene expression, suppressive subtractive hybridization,
other cell biology, biochemical, and chemiluminescence techniques as
well as xenograft and transgenic models of disease and in situ studies
on human tissues approaches to address many questions as they relate to
prostate tumorigenesis. Using a super-repressor I kappa B adenoviral
delivery approach, the lab plans to evaluate the role of inhibiting the
activation of the nuclear factor NF-kappa B in enhancing
radio/chemosensitization and apoptosis of prostate tumor cells.
Analysis of the expression and function of these genes should allow for
a more in depth understanding of the processes controlling prostate
tumor growth, invasion and metastasis. The ultimate aim is on
developing new diagnostic tools and potential therapeutic applications
using a gene therapy approach (pharmacogenomics).
Recent Publications:
-
Sikka SC. (2001) Relative Impact of
Oxidative Stress on Male Reproductive Function. Current Medicinal Chem 1: 851-862.
- Rajasekaran M, Hellstrom
WJG, Sikka SC. (2001) Nitric oxide
induces oxidative stress and mediates cytotoxicity to human cavernosal
cells in culture. J Androl 22:
34-39.
- Sikka SC, Champion H, Bivalacqua TJ,
Estrada L, Wang R, Rajasekaran M, Aggarwal B, Hellstrom
WJG. (2001) Role of genitourinary inflammation of infertility:
detrimental effect of lipopolysaccharide (LPS) and nterferon-gamma on
human spermatozoa. Int J Androl
(in press).
- Nguyen A, Jing S, Mahoney S, Davis R,
Sikka SC, Agrawal
KC, Abdel-Mageed AB. (2000) In
vivo gene expression profile analysis of metallothionein in renal cell
carcinoma. Cancer Letters 160:
133-140.
- Bivalacqua TJ, Champion HC, Mehta YS, Abdel-Mageed
AB, Sikka SC, Ignarro LJ, Kadowitz
PJ, Hellstrom
WJG. (2000) Adenoviral gene transfer of endothelial nitric oxide
synthase (eNOS) to the penis improves age-related erectile dysfunction
in the rat. Int J Impotence Res
12: 8-17.
- Armstrong JS, Rajasekaran M, Chamulitrat W, Gatti P, Hellstrom
WJG, Sikka SC. (1999)
Characterization of reactive oxygen species induced effects on human
spermatozoa movement and energy metabolism. Free Radical Biol Med 26(7/8):
869-80.
Sudesh K. Srivastav, Ph.D.
Assistant Professor of
Biostatistics, Tulane
School of Public Health and Tropical Medicine
TCC Associate Member
ssrivas@tulane.edu
(504) 988-2472, (504) 988-1706 fax
1430 Tulane Ave., Box SL-16, New Orleans, LA 70112-2699
Homepage on the Biostatistics website:
http://www.biostatistics.tulane.edu/bio_pages/faculty_bio/srivatav.html
Biographical information:
Dr. Srivastav received his masters degree in Statistics from Indian
Statistical Institute in 1988 and another masters degree in Applied
Mathematics from New Jersey Institute
of Technology, New Jersey in 1990. He received his Ph.D. in Design
of Experiments from Old Dominion
University, Virginia in 1996 and in the same year he took a faculty
position at University of
California at San Francisco as Assistant Adjunct Professor in
Biostatistics. In 1999 he joined the Department of Biostatistics at
Tulane's School of Public Health
and Tropical Medicine. He became an honorary fellow at the Center
of Mathematical Sciences at the University
of Wisconsin, Madison in summer 2000. Dr. Srivastav will be a
research fellow at the Department of Statistics at Stanford University during summer
2001. Dr. Srivastav has published numerous papers in both theoretical
and applied statistical and medical journals. His research is focussed
on methodology that is devoted toward establishing the optimality and
construction of block designs under a different set of parameters
(number of treatments, number of blocks and block size, etc). This
research will provide a simple classification scheme of study designs
that can be useful in the field of health science, agricultural science
and industrial engineering.
Recent Publications:
-
Morgan JP, Srivastav SK. (2000) On
the Type-1 optimality of Nearly Balanced Incomplete Block Designs with
small Concurrence range. Statistica
Sinica 10(4): 1091-1116.
- Bonel HM, Schneider P, Seemann MD, Hugli R, Srivastav SK, Lodemann KP, Reiser M. (2001)
MR imaging of the wrist in rheumatoid arthritis using gadobenate
dimeglumine. Skel Radiol 30:
15-24.
- Prevrhal S, Fuerst T, Fan B, Njeh CF, Hans D, Uffmann M, Srivastav SK, Genant HK. (2001) What Does
Quantitative Ultrasound of the Tibia Measure? Osteop Int 12(1): 20-26.
- Hans D, Srivastav SK, Njeh CF,
Singal C, Wu C, Genant HK. (1999) Does combining the results from
multiple bone sites measured by a new Quantitative Ultrasound improve
discrimination of hip fracture? J
Bone Min Res 14(4): 644-651.
William C. Steinmann, M.D.
Professor of Medicine
Section of Internal Medicine
TCC Associate Member
wsteinm@tmpop.som.tulane.edu
(504) 988-7518, (504) 988-2860 fax
1430 Tulane Ave., Box SL-18, New Orleans, LA 70112-2699
Specialties, publications, and research: Screening and treatment of
tumors
Alan Stolier, M.D.
Professor of Surgery
TCC Associate Member
astolier@tulane.edu
(504) 988-3311, (504) 988-6114 fax
1430 Tulane Ave., Box SL-22, New Orleans, LA 70112-2699
Biographical information:
Alan Stolier, M.D., is currently Professor of Surgery at Tulane University School of Medicine.
Following his surgical internship at the University of Virginia
Hospital he completed his general surgical training at Louisiana State University. He then
completed fellowships in surgical oncology at both the M.D. Anderson Hospital and Tumor
Institute in Houston, Texas, and at the Hammersmith
Hospital in London, England. Beginning in 1993, he limited his
practice to breast surgery and at that time became the first medical
director of the Breast Cencer at Memorial
Hospital in New Orleans as well as the Lieselotte Tansey Breast
Center at the Ochsner Clinic
Foundation. He is a Fellow of the American
College of Surgeons and the Society
of Surgical Oncology. He is a member of the American Society of Breast Disease, American Society of Clinical Oncology,
and Past President of the James D. Rives Surgical Society. His most
recent publications and interests have centered on hereditary breast
cancer and accelerated partial breast irradiation.
Karen A. Sullivan, Ph.D.
Research Professor of Medicine
Director of Histocompatability and Immunogenetics
TCC Associate Member
karens@tulane.edu
(504) 988-5259, (504) 988-3636 fax
1430 Tulane Ave., Box SL-75, New Orleans, LA 70112-2699
Biographical information:
Dr. Sullivan received her B.S. in 1966 from the Massachusetts College of Liberal Arts
and her Ph.D. in 1973 from Duke
University. She completed her postdoctoral research from 1973-1975
at the McIndoe Memorial Research Unit, Blond Laboratories, Queen
Victoria Hospital, Sussex, England and was a postdoctoral fellow from
1975-1978 in the Division of Laboratories and Research, New York State
Department of Health. Dr. Sullivan's Histocompatibility and
Immunogenetics Laboratory provides histocompatibility testing support
for the Tulane Multi-Organ Transplant programs which include kidney,
liver, heart and pancreas. The laboratory also provides allogenic and
autologous bone marrow transplantation. This support includes typing
for the genes and antigens of the Major Histocompatability Complex
(HLA) in order to determine the level of phenotypic and/or genetic HLA
identity between individuals. It also includes crossmatching between
recipient sera and donor lymphocytes; antibody screening of patient
sera to determine the level of sensitization and specificity of
antibodies to HLA antigens in the general population. The
Histocompatability and Immunogenetics Laboratory also performs
immunophenotyping of lymphocyte subsets. The laboratory also provides
HLA typing for disease association and other non-transplant relateed
reasons, including research. The laboratory has extensive expertise in
HLA typing for Class I and Class II antigens by serological and
molecular methodology, two- and three-color flow cytometry for
immunophenotyping, antibody screening and crossmatching, enzyme-linked
immunosobant assays for the detection and identification of antibodies
specific for HLA antigens, isolation and viable freezing of PBMC and in
vitro tissue culture, lymphoproliferative assays to mitogens and recall
antigens, mixed lymphocyte culture assays and cell-mediate cytotoxic
assyas for CTL and NK cell activity.
Recent Publications:
-
Jaspan JB, Breyer-Ash M, Sullivan KA,
Lopez ML, Wolfe MA, Clejan S, Yan C,
Ahmed B, Garry RF. (1996) The
interaction of type-A retroviral particle and class II HLA
susceptibility gees in the pathgenesis of Graves' disease. J Clin Endo Metab 81: 2271-2279.
- Sullivan KA, Wolfe MA, Lopez M,
Jaspan JJ, Breyer-Ash M. (1997) First report of recombination between
the HLA-DR and HLA-DQ loci within a family. Hum Immunol 57: 37-43.
- Sullivan KA, Kipps TS. (2000)
"Human leukocyte and platelet antigens". In Williams' Hematology,
6th Edition. Beutler, Lichtman, Coller, Kipps and Seligsohn, Eds.
McGraw-Hill.
- Sullivan KA. (2000) "HLA and
transplantation". In Molecular Tying 2000: A Technical Manual
for Histocompatibility Laboratories. C.H. Manning, B. Burgess and F.E.
Ward, Eds. Southeastern Organ Procurement Foundation.
- Madan AK, Slakey DP, Becker A, Gill JI, Heneghan JL, Sullivan KA, Cheng S. (2000) Treatment of
Antibody-mediated accelerated rejection using plasmapheresis. J Clin Apher 15: 180-183.
A B C D E
F G H I J
K L M N
O
P Q R S
T U V W X
Y Z
Return to the top of this page.
Return to the Tulane Cancer
Center homepage.
Calendars
Clinical Trials
Faculty
Links
Location
News
Search
Site index
This page is http://www.som.tulane.edu/cancer/TCCnames/facs.html
This page was last updated on
Tulane Cancer Center, Box SL-68
1430 Tulane Avenue
New Orleans, Louisiana 70112-2699
(504) 988-6060, fax (504) 988-6077
http://www.som.tulane.edu/cancer