Program Director/Principal Investigator :

BIOGRAPHICAL SKETCH

NAME
Cheryl L. Willman, M.D. / POSITION TITLE
Professor of Pathology and Medicine
The Maurice and Marguerite Liberman Distinguished Chair in Cancer Research
Director and CEO, UNM Cancer Center
University of New Mexico Health Sciences Center
eRA COMMONS USER NAME
cwillman
EDUCATION/TRAINING
INSTITUTION AND LOCATION / DEGREE
(if applicable) / YEAR(s) / FIELD OF STUDY
St. Olaf College, Northfield, MN /

BA

/ 1977 / Chemistry
Mayo Medical School, Rochester, MN /

MD

/ 1981 / Medicine
University of New Mexico, Albuquerque, NM /

Residency

/ 1984 / Anatomic Path/Hemepath
UNM, Albuquerque, NM; HHMI/ U Wash, Seattle, WA /

Fellowship

/ 1986-1989 / NIH Physician Scientist

PHS 398/2590 (Rev. 06-09) Page Biographical Sketch Format Page

Program Director/Principal Investigator :

A. Personal Statement

My laboratory is focused on the use of comprehensive genomic technologies, next generation sequencing methods, and computational and statistical modeling tools to discover new genetic abnormalities in acute leukemia that may serve as targets for diagnosis or therapy. I lead multidisciplinary teams of clinicians and scientists who are focused on: 1) translating molecular discoveries (prognostic genes and signatures) to the clinical setting (under CLIA and in the context of NCI clinical trials) where they are being used as integral or integrated markers for patient screening and therapeutic targeting; and, 2) developing new therapeutic approaches, including nanotherapeutics, to target these mutations in pre-clinical animal models and ultimately human clinical trials. I am PI of a NCI SPECS II Grant, a NCI Nanotechnology Platform Partnership Grant, a Lead Investigator in the NCI TARGET Project in High-Risk ALL (www.target.cancer.gov), a Project PI in a newly funded LLS SCOR in High Risk Leukemia, and a Project PI in a newly funded grant from the St. Baldrick’s Foundation which supports integral correlative studies in a COG high risk ALL trial where our gene expression classifiers and next generation sequencing methods are being used for patient molecular characterization and therapeutic targeting. As Director of the UNM Cancer Center and a member of the NCI Board of Scientific Counselors and the NCI National Clinical Trials Network Working Group, I have extensive experience in development, leadership, and evaluation of NCI Cancer Centers and the NCI Clinical Trials Program.

B. Positions and Honors

1984-1989 NIH Physician Scientist Training Award NIDDK: K11-DK-01284 (Mentors: T.B. Tomasi, MD, PhD, UNM; Roger M. Perlmutter, M.D., Ph.D., HHMI, University of Washington)

1986-1991 Assistant Professor, Pathology, UNM School of Medicine, Albuquerque, NM

1987-2010 Chair, Southwest Oncology Group, Leukemia Translational Medicine Committee

1991-1995 Associate Professor of Pathology with Tenure, UNM School of Medicine

1992-1996 National Institutes of Health, Hematology-2 Study Section

1995-Present Professor, Pathology and Medicine, UNM School of Medicine

1996-2001 PI & Program Director, UNM Howard Hughes Medical Institute Research Resources Program

1998-Present Children’s Oncology Group, Leukemia Reference Laboratories; ALL Executive Committee

1998-2002 Councilor; Executive Committee, American Society of Hematology

1999-Present Director and CEO, University of New Mexico Cancer Center

2000-2005 National Institutes of Health, Hematology 2 / Hematopoiesis Study Sections; Chair (2003-05)

2000-09, 2012- Medical and Scientific Advisory Board, Leukemia and Lymphoma Society of America

2002-2008 Scientific Advisory Board; Chair, Bioscience Review Panel, Sandia National Laboratories

2007-2010 Board of Directors, American Association of Cancer Institutes (AACI)

2010-Present NCI Board of Scientific Counselors; Scientific Advisory Committee – NCI Frederick National Cancer Research Laboratory

2010-Present NCI Steering Committee on the Hematologic Malignancies: Acute Lymphoblastic Leukemia (ALL) and Acute Myeloid Leukemia (AML) Working Groups

2012-Present Member, External Advisory Board, NCI Center to Reduce Cancer Health Disparities

2012-Present Member, NCI National Clinical Trials Network Working Group

Honors: 1973: State of Iowa Scholar. 1977: St. Olaf, David E. Gaardner Award-Chemistry; Phi Beta Kappa. 1985: Stowell-Orbison Research Award, International Academy of Pathology. 1994: Benjamin Castleman Award, International Academy of Pathology. 1995: Women in Science Hall of Fame, US Dept. of Energy. 1998: President, Association for Molecular Pathology. 1998: Young Investigator Award, US-Canadian Division of the International Academy of Pathology. 2001:16th Annual Governor’s Award for Outstanding New Mexico Woman. 2006: New Mexico Distinguished Public Service Award. 2012: New Mexico Award for Technology/Engineering; 2013: New Mexico “La Estrella” Award, for New Mexico’s most outstanding woman leader.

C. Selected Peer-Reviewed Publications (From > 220)

1.  Mullighan CG, Zhang J, Harvey RC, Schulman BA, Phillips LA, Su X, Devidas M, Atlas SR, Chen IM, Clifford R, Gerhard D, Carroll WL, Reaman GH, Smith M, Downing JR, Hunger SP, and Willman CL. 2009. JAK mutations in high risk childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA. 2009. Jun 9; 106(23):9414-8. PMCID: PMC2695045

2.  Zhang J, Mullighan CG, Harvey RC, Wu G, Chen X, Edmonson M, Buetow KH, Carroll WL, Chen I-M, Devidas M, Gerhard DS, Loh ML, Reaman GH, Relling MV, Camitta BM, Bowman WP, Smith MA, Willman CL#, Downing JR#, and Hunger SP.# (# senior authors who contributed equally). Mutations in the RAS signaling, B-cell development, TP53/RB1, and JAK signaling pathways are common in high risk B-precursor childhood acute lymphoblastic leukemia: A report from the Children’s Oncology Group NCI TARGET Project. 2011. Blood. 118(11):3080-7. PMCID: PMC3175785

3.  Ashley CE, Carnes CE, Phillips GK, Padilla D, Brown PA, Hanna TN, Liu J, Comyford B, Carroll N, Jiang X, Spielman I, Willman CL, Petsev DN, Evans DG, Chackerian B, Wharton W, Peabody DS, and Brinker CJ. The targeted delivery of multicomponent cargoes to cancer cells by nanoporous particle-supported lipid bilayers. Nature Materials. 2011. May; 10(5):389-97. Epub, 2011, April 17. PMCID: PMC3287066. (Cover).

4.  Ashley CE, Carnes EC, Phillips GK, Durfee PN, Buley M, Padilla DP, Phillips B, Carter MC, Willman CL, Brinker CJ, Chackerian B, Wharton, W, and Peabody DS. Cell-specific delivery of diverse cargos by bacteriophage MS2 virus-like particles. ACS Nano. 2011. Jul 26; 5(7):5729-45. (Cover). PMCID: PMC3144304.

5.  Kang H, Wilson CS, Harvey RC, Chen IM, Murphy MH, Atlas SR, Bedrick EJ, Devidas M, Carroll AJ, Robinson BW, Stam RW, Valsecchi MG, Pieters R, Heerema NA, Hilden JM, Felix CA, Reaman GH, Camitta B, Winick N, Carroll WL, Dreyer ZE, Hunger SP, Willman CL. Gene expression profiles predictive of outcome and age in infant acute lymphoblastic leukemia: a Children's Oncology Group study. Blood. 2012 Feb 23;119(8):1872-81. PMCID: PMC3293641.

6.  Ashley CA, Carnes EC, Epler KE, Padilla DP, Phillips GK, Carroll NK, Castillo RE, Wilkinson DC, Wilkinson BS, Burgard CA, Kalinich RM, Townson JL, Chackerian B, Willman CL, Peabody DS, Pestev DN, Wharton W, and Brinker CJ. Delivery of Small Interfering RNA by Peptide-Targeted Mesoporous Silica Nanoparticle-Supported Lipid Bilayers. ACS Nano. 2012. Mar 27; 6(3):2174-88. PMCID: PMC3332089

7.  Xu H, Cheng C, Devidas D, Pei D, Fan Y, Yang W, Neale G, Scheet P, González-Burchard E, Torgerson DG, Eng C, Dean M, Antillon F, Winick NJ, Martin PL, Willman CL, Camitta BM, Reaman GH, Carroll WL, Loh M, Evans WE, Pui CH, Relling MV, Hunger SP, and Yang JJ. ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment of childhood acute lymphoblastic leukemia. J Clinical Oncol. 2012. Mar 1; 30(7):751-7. Epub Jan 30. PMCID: PMC3295551.

8.  Chen IM, Harvey RC, Mullighan CG, Gastier-Foster J, Wharton W, Kang H, Borowitz MJ, Camitta BM, Carroll AJ, Devidas M, Pullen DJ, Payne-Turner D, Tasian SK, Reshmi S, Cottrell CE, Reaman GH, Bowman WP, Carroll WL, Loh ML, Winick NJ, Hunger SP, Willman CL. Outcome modeling with CRLF2, IKZF1, JAK, and minimal residual disease in pediatric acute lymphoblastic leukemia: a Children's Oncology Group study. Blood. 2012 Apr 12;119(15):3512-22. PMCID: PMC3325039.

9.  Tasian SK, Doral MY, Mullighan CG, Borowitz MJ, Wood BL, Chen IM, Harvey RC, Gastier-Foster JM, Willman CL, Hunger SP, and Loh ML. Aberrant JAK/STAT and PI3K/mTOR pathway signaling occurs in human CRLF2-rearranged B-precursor acute lymphoblastic leukemias. 2012. Blood. July 26; 120(4):833-42. PMCID: PMC3412346

10.  Roberts KG, Morin R, Zhang J, Hirst M, Zhao Y, Su, X, Chen S-C, Payne-Turner D, Churchman M, Chen X, Harvey R, Kasap C, Yan C, Becksfort J, Finney RP, Teachey D, Maude S, Tse, K, Moore R, Jones S, Mungall K, Birol I, Edmonson M, Hu Y, Buetow KE, Chen I-M, Carroll WL, Wei L, Ma J, Kleppe M, Levine R, Garcia-Manero G, Larson E, Shah N, Devidas M, Reaman G, Smith M, Paugh S, Evans WE, Grupp S, Jeha S, Pui C-H, Gerhard DS, Downing JR, Willman CL, Loh M, Hunger SP, Marra M, Mullighan CG. Novel genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia. Cancer Cell. 2012. Aug 14; 22(2):153-66. PMCID: PMC3422513.

11.  Maude SL, Tasian SK, Vincent T, Hall JW, Sheen C, Roberts KG, Seif AE, Barrett DM, Chen IM, Collins JR, Mullighan CG, Hunger SP, Harvey RC, Willman CL, Fridman JS, Loh ML, Grupp SA, and Teachey DT. Targeting Jak1/2 and mTOR in murine xenograft models of Ph-like acute lymphoblastic leukemia. Blood. 2012 Oct 25; 120(17):3510-8. PMCID: PMC3482861.

12.  Yang JJ, Cheng C, Devidas M, Cao X, Campana D, Yang W, Fan Y, Neale G, Cox N, Borowitz MJ, Winick NJ, Martin PL, Willman CL, Bowman WP, Reaman GH, Carroll WL, Loh M, Evans WE, Pui C-H, Hunger SP, and Relling MV. Genome-wide association study identifies germline polymorphisms associated with relapse of childhood ALL. Blood. 2012 Nov 15; 120(20):4197-204. PMCID: PMC3501717

13.  Loh ML, Zhang J, Mullighan CG, Harvey RC, Roberts K, Payne-Turner D, Kang H, Wu G, Chen X, Becksfort J, Edmonson M, Buetow KH, Carroll WL, Chen I-Ming, Devidas M, Gerhard DS, Bowman P, Larsen E, Raetz E, Smith M, Downing JR, Willman CL, and Hunger, SP. Tyrosine kinome sequencing of high risk pediatric ALL: TARGET Project Update. Blood. 2013 Jan 17;121(3):485-8. PMCID: PMC3548168

14.  Parham RR, Geng H, Chen Z, Chan LN, Jumaa H, Melnick A, Paietta E, Carroll WL, Willman CL, Lefebvre V, and Müschen M. SOX4 enables oncogenic survival signals in acute lymphoblastic leukemia. Blood. 2013 Jan 3;121(1):148-552012. PMCID: PMC3538327

15.  Hsieh YT, Gang EJ, Geng H, Park E, Huantes S, Chudziak D, Dauber K, Schaefer P, Scharman C, Shimada H, Shojaee S, Klemm L, Parameswaran R, Loh M, Kang ES, Koo HH, Hoffman WK, Andrade J, Crooks GM, Willman CL, Müschen M, Papayannopoulou T, Heisterkamp N, Bönig H, Kim YM. Integrin alpha4 blockade sensitizes drug resistant pre-B cell acute lymphoblastic leukemia to chemotherapy. Blood. 2013 Mar 7;121(10):1814-8. PMCID: PMC3591800

D. Research Support

Ongoing Research Support

2 P30 CA118100 (PI: Willman) 09/01/10-08/31/15

NCI

University of New Mexico Cancer Center Support Grant

This Cancer Center Support Grant (CCSG) provides NCI support for leadership administration, programs, shared resources, clinical trials support, and developmental funds for the UNM NCI-Designated Cancer Center.

1 U01 CA151792 (Contact PI: Willman, Multi PI: Brinker) 08/01/10-08/31/15

NCI

Nanotechnology Platform Partnership: Peptide-Directed Protocells and Virus-Like Particles: New Nanoparticle Platforms for Targeted Cellular Delivery of Multicomponent Cargoes

The goal of this project is to develop nanoparticle platforms to target delivery of a variety of different cargos to acute lymphoblastic leukemia cells and solid tumors (ovarian cancer, hepatocellular carcinoma).

1 U01 CA157937 (Contact PI: Willman, Multi PI: Hunger) 08/01/11-07/31/16

NCI

SPECS II: Molecular Signatures for Outcome Prediction and Therapeutic Targeting in ALL

The goal of this project is to develop gene expression classifiers and next generation sequencing methods as integral and integrated markers for targeted therapy in NCI Sponsored Clinical Trials in COG, ECOG, and the Alliance.

Leukemia & Lymphoma Society SCOR (PI: Carroll) 10/01/13-08/31/18

LLS

Project 4: Targeted Nanotherapeutics for ALL Therapy (PI: Willman; Co-PIs: Brinker (UNM), Grupp (CHOP/UPENN))

SCOR Project 4 goals are focused on the production and synthesis of novel therapeutic nanocarriers (“protocells”) targeted to either CRLF2 or CD19; such protocells will encapsidate imaging agents that allow monitoring of their tracking and uptake in vitro and in vivo and/or therapeutic agents directed towards ALL cells

St. Baldrick’s Foundation (PI: Hunger) 07/01/13-06/30/18

Testing Targeted Therapy in Philadelphia Chromosome-like (Ph-like) ALL

The UNM component (Project PI: Willman) is focused on the implementation of retrospective and prospective screening of pediatric ALL patients classified as high or standard risk for the Ph-like (BCR-ABL1-like) genotype, using a gene expression-based molecular classifier developed at UNM which has been converted to a low density array (LDA) card which can be utilized in a CLIA-approved clinical diagnostic setting in the context of NCI-sponsored trials. Application to FDA for an IVD is in progress so that this classifier and next generation sequencing methods can be used as integral markers in a new high risk ALL trial in COG where ALL patients positive in the LDA screen will be further characterized molecularly using transcriptomic sequencing methods (RNAseq) and then targeted to combination therapies incorporating specific tyrosine kinase inhibitors.

PHS 398/2590 (Rev. 06/09) Page Continuation Format Page