Arthur E. Frankel, M.D.

Primary Office

Temple Clinic
254-724-1895

Arthur E. Frankel, M.D.

  • Director, Cancer Center
  • Director, Division of Hematology/Oncology
  • Director, Cancer Research Institute


Hematologic Malignancies, Hematology, Hematology and Oncology, Oncology

Faculty Rank - Texas A&M Health Science Center College of Medicine

Professor of Medicine

Education

  • Harvard Medical School, Harvard, Cambridge, MA, M.D., 1973
  • Harvard College, Harvard, Cambridge, MA, A.B., 1969

Specialty Training

  • Fellowship in Oncology, Stanford University, Stanford, CT, 1982
  • Residency in Medicine, Stanford University, Stanford, CT, 1980
  • Research Scientist, NIH, 1978
  • Internship in Medicine, Yale University, New Haven, CT, 1974

Scott & White Appointment

July 1, 2005

Board Certification

American Board of Internal Medicine, Medical Oncology, Hematology

Publications and Research

  • Alfano RW, Leppla SH, Liu S, Bugge TH, Duesbery NS, Frankel AE. Potent inhibition of tumor angiogenesis by the matrix metalloproteinase-activated anthrax lethal toxin: implications for broad anti-tumor efficacy.  Cell Cycle 7[6], 745-749. 2008.
  • Ding Y, Boguslawski EA, Berghuis BD, Young JJ, Zhang ZF, Hardy K, Furge K, Kort E, Frankel AE, Hay RV, Resau JH, Duesbery NS. Mitogen-activated protein kinase kinase signaling promotes growth and vascularization of fibrosarcoma.  Molecular Cancer Therapeutics 7[3], 648-658. 2008.
  • Frankel AE, Liu JS, Rizzieri D, Hogge D. Phase I clinical study of diphtheria toxin-interleukin 3 fusion protein in patients with acute myeloid leukemia and myelodysplasia.  Leukemia and Lymphoma 49[3], 543-553. 2008.
  • Horita H, Frankel AE, Thorburn A. Acute-myeloid-leukemia-targeted toxins kill tumor cells by cell-type-specific mechanisms and synergize with TRAIL to allow manipulation of the extent and mechanism of tumor cell death.  Leukemia 22[3], 652-655. 2008.
  • Liu S, Wang H, Currie BM, Molinolo A, Leung HJ, Moayeri M, Basile JR, Alfano RW, Gutkind JS, Frankel AE, Bugge TH, Leppla SH. Matrix metalloproteinase-activated anthrax lethal toxin demonstrates high potency in targeting tumor vasculature.  Journal of Biological Chemistry 283[1], 529-540. 2008.
  • Rouleau C, Menon K, Boutin P, Guyre C, Yoshida H, Kataoka S, Perricone M, Shankara S, Frankel AE, Duesbery NS, Woude GV, Biemann HP, Teicher BA. The systemic administration of lethal toxin achieves a growth delay of human melanoma and neuroblastoma xenografts: Assessment of receptor contribution.  International Journal of Oncology 32[4], 739-748. 2008.
  • Read more publications.

Professional Activities

  • American Association of Cancer Research
  • American Society of Hematology
  • American Society of Clinical Oncology

Awards

  • John Harvard Award
  • Phi Beta Kappa
  • Churchill Fellowship
  • Summa Cum Laude
  • Detur


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