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Hollings Scholars & Fellows

These awardees are advancing cancer knowledge with support from programs at MUSC Hollings Cancer Center.

Hollings Clinical Scholars

Maggie Westfal, M.D.

Assistant Professor, Surgery
westfal@musc.edu

Implementation of a Pilot Program for Opportunistic Salpingectomy at the Time of Gastrointestinal Surgery at MUSC: An Evaluation of Patient and Provider Knowledge and Attitudes

The goal of this research is to assess the knowledge and attitudes of patients and GI surgeons regarding opportunistic salpingectomy (removal of fallopian tubes to prevent ovarian cancer) and to implement an opportunistic salpingectomy pilot program to assess feasibility and outcomes at MUSC.

Kathryn E. Engelhardt, M.D.

Assistant Professor, Surgery
engelhar@musc.edu

Development and Implementation of a Novel Shared Decision-Making Tool to Support Cancer Care Delivery Concordant with Patient Treatment Preferences

Most shared-decision making (SDM) interventions are designed to improve provider delivery of knowledge to the patient. I aim to improve the balance of information in SDM models by empowering patients to share their care goals with providers. I will (1) study the process of implementation of a previously developed SDM tool and (2) develop a patient-centered SDM tool to facilitate patients sharing what their care goals are, as they undergo treatment for lung cancer.

Clinical Scholar Award

Postdoctoral & Clinical Fellowship Awardees

Ozge Saatci, Ph.D.

LOWVELO Post-doctoral Fellow

Project: Roles of Aminoacyl tRNA Synthetases in Tumor Progression

Mentor: Ozgur Sahin, Ph.D.

My research interests focus on discovering novel mechanisms of therapy resistance and metastasis, and preclinical testing of novel therapeutic approaches to treat aggressive breast cancers. I had an extensive training in cancer cell biology, functional transcriptomics/bioinformatics, translational medicine, and drug discovery during my postgraduate studies.

Alessandro Zuccotti, Ph.D.

LOWVELO Post-doctoral Fellow

Project: Therapeutic Targeting of HSP70 in Colorectal Cancer

Mentor: Tim Barnoud, Ph.D.

Colorectal cancer (CRC) remains one of the most diagnosed cancers world-wide. In addition, it is estimated that over 50,000 people in the United States will die from CRC in 2024. Despite the emergence of new targeted and immune based therapies, the five-year survival rate for patients with metastatic CRC remains below twenty percent. The molecular chaperone known as ‘heat shock protein 70’ (HSP70) is markedly over-expressed in CRC and is significantly associated with poor survival.

Based on these clinical findings, we developed a unique HSP70 inhibitor that is highly potent in CRC cells but is significantly less toxic to normal colon epithelial cells and tissues. The long-term goal of this research project is to test our unique HSP70 inhibitor in pre-clinical models of CRC.

Importantly, we plan to develop new combination strategies for the hardest to treat subtypes of CRC, including mutant B-RAF and mutant p53 driven CRC. We will also determine the mechanism by which HSP70 inhibition promotes cell death in CRC. We hope that the successful completion of this project will advance our fundamental understanding of HSP70 in CRC.

Postdoc & Clinical Fellowship

Graduate Fellowship Awardees

Kubra Calisir Unsal

LOWVELO HCC Graduate Fellow

Project: Targeting Triple Negative Breast Cancer with High Chromosomal Instability

Mentor: Ozgur Sahin, Ph.D.

My research focuses on triple-negative breast cancer (TNBC), which accounts for 10–15% of all breast cancer cases and is associated with a more aggressive phenotype, earlier recurrence, and poorer overall survival compared to non-TNBC subtypes.

Chemotherapy remains the primary treatment option; however, most TNBC patients ultimately develop resistance. TNBC is characterized by high chromosomal instability (CIN)—a hallmark of aggressive tumors that is poorly tolerated by normal cells but frequently exploited by cancer cells. CIN contributes to poor prognosis, metastasis, and therapeutic resistance. Thus, effective targeted therapies for CIN-high TNBC remain lacking. Through my work, we have identified TACC3, a member of the transforming acidic coiled-coil protein family, as a novel vulnerability in TNBC.

My current study aims to elucidate the molecular mechanism of TACC3 in TNBC, advancing our understanding of CIN-driven cancers and paving the way for new therapeutic strategies.

Pritika Shahani

LOWVELO HCC Graduate Fellow

Project: Identifying translational drug combinations for medulloblastoma treatment

Mentor: Jezabel Rodriguez Blanco, Ph.D.

Brain tumors are the leading cause of cancer-related deaths in children, with medulloblastoma (MB) being the most common. MB is classified into four molecular subgroups: WNT, Sonic Hedgehog (SHH), Group 3, and Group 4. This classification has improved our understanding of these malignancies and allowed for the development of targeted therapies.

Despite these advances, most children with MB are still treated with standard-of-care protocols, including surgery followed by radiation and chemotherapy targeting highly proliferative cells. While these treatments can be curative, they leave survivors with long-term side effects.

Targeted therapies offer a less toxic alternative, but many oncogenic drivers in MB, such as the Glioma-associated (GLI) oncogene, are difficult to target directly. Bromodomain and Extra-Terminal (BET) inhibitors (BETi) have shown promise by indirectly blocking the transcriptional activity of this oncogene, thereby reducing tumor growth in the SHH MB subgroup. However, dose-limiting toxicities observed in clinical studies threaten BETi translation. My research in SHH MB models suggests that combining drugs that synergize with BETi can reduce the required BETi dose, minimizing toxicities while preserving efficacy.

My research is aimed at finding drug combinations that by acting synergistically allow a reduction in BETi dosing, minimizing toxicities while preserving efficacy. The successful completion of this project will pave the way for clinical trials aimed at improving outcomes for children with SHH MB. Moreover, given the involvement of GLI in driving other malignancies, this therapeutic approach could be easily extended beyond MB patients.

Graduate Fellowship

T32 ITOS Program Fellows

Tarah Trebino, Ph.D.

Mentor: John O'Bryan, Ph.D.

Project Title: Mechanisms of RAS-mediated oncogenic signaling

Research Interests: cancer research, biochemical/biophysical methods, signaling mechanisms, therapeutic developments.

Research Aims: Investigate current mechanisms of RAS signaling and inhibition with RAS monobodies and small-molecule inhibitors.

Allison Reno, Ph.D.

Mentors: Denis Guttridge, Ph.D., Casey Langdon, Ph.D.

Project Title: 3D Organoid Models of Pediatric Sarcomas

Research Interests: My research interests are in 3D human culture modeling for pharmaceutical screening and tissue microenvironment modeling to understand how the 3D environment alters the molecular and pharmacological impact of current and future cancer treatments.

Research Aims: My research aims to develop and utilize 3D sarcoma organoids as a research tool for studying tumor microenvironments and pharmaceutical drug efficacy in pediatric sarcomas. The goal of the research is to first investigate and develop a sarcoma organoid model system that will be representative of native tissues found in pediatric sarcoma patients. Later we will use that model to examine the effects of drug response in a 3D environment as well as investigate the molecular and structural components, such as angiogenesis and protein transport, of the 3D tumor microenvironment in pediatric sarcomas.

Carlos Gomez, Ph.D.

Mentor: Antonis Kourtidis, Ph.D.

Project Title: A mechanosensitive RNAi machinery regulates pro-tumorigenic transformation in the colon

Research Interests: My research interests revolve around understanding the interplay between mechanics and biological signaling in cancer. I am particularly interested in how these two influence each other as cancer progresses. By extension, I am also interested in developing therapeutics aiming at either biological or mechanical properties of cancer and investigating their effect on this interplay.

Research Aims: I aim to further our understanding of the interplay between biological signaling and mechanics in cancer. In my doctoral training, I studied how the mechanical properties of cancer change as tumors begin to invade. In my upcoming post-doctoral experience, I aim to delve deeper into the molecular machineries that regulate these mechanical changes and that eventually lead to the progression of cancer. Specifically, I will be determining how PLEKHA7-associated RNAi regulates extracellular remodeling and cell behavior.

Kristy Thomas, Ph.D.

Mentor: Jessica H. Hartman, Ph.D.

Project Title: Cytochrome P450 2E1 (CYP2E1) and its role in cancer metabolism

Research Interests: My research interests include nutrition, obesity, and metabolism (metabolic syndrome). My dissertation research focused on maternal and infant nutrition and metabolism. I specifically looked at maternal obesity and how maternal obesity impacts breast milk short chain fatty acid and microbiome profiles, preterm infant fecal short chain fatty acid and microbiome profiles. During my Ph.D. studies, my research focused on metabolic syndrome in several groups: female mice with alcoholic liver disease, male mice with non-alcoholic liver disease caused by the standard American diet (SAD) and men with HIV on PrEP, which has been known to cause malabsorption.

Research Aims:

  1. Determine the sensitivity of well-differentiated and poorly differentiated hepatocellular carcinoma cells expressing CYP2E1 to palmitate and iron.
  2. Establish if the mechanism of cell death in hepatocellular carcinoma cells is through ferroptosis or another mechanism.
  3. Compare the findings from Aims 1 and 2 to several colorectal cancer cell lines which are known to be resistant to undergoing ferroptosis.

Farah Alfatyan, Ph.D.

Mentors: Tim Barnoud, Ph.D. and David Long, Ph.D.

Project Title: Tumor extrinsic roles of HSP70 and p53 in cancer

Research Interests: Passionate about exploring the immunological basis of cancer and testing and developing effective cancer immunotherapies. My research interest lies in exploring and unravelling the complexities of the tumor microenvironment and/or the immune system.

Research Aims: HSP70 and mutant p53 have been implicated in the initiation, progression, and metastasis of a wide range of human cancers. However, the tumor extrinsic roles of these proteins have not been fully investigated. My long-term goals are to better understand the molecular mechanisms by which HSP70 and mutant p53 promote cancer by regulating the tumor microenvironment (TME) in gastrointestinal cancers, with a particular focus on pancreatic and liver cancer.

Ian Padykula, Ph.D.

Mentor: John Wrangle, M.D.

Project Title: Topical AAV-based gene therapy for the treatment of locally recurrent, surgically refractory cervical cancer

Research Interests: Investigating the trafficking of lymphoid cells to mucosal tissues in response to tumorigenesis and infectious diseases.

Research Aims: The aim of my research is to develop an AAV-vectored therapeutic for the targeted delivery of immunotherapies to cervical cancer cells. By designing payloads tailored to the mucosal tissue environment, we will leverage existing immunotherapies to better direct cytotoxic cells to solid tumors at these boundaries.

Lyndsay E. A. Young, Ph.D.

Mentor: Richard R. Drake, Ph.D.

Project Title: Advancements in glycogen detection and spatial profiling reveals a new therapeutic for Ewing sarcoma: a non-traditional glycogen storage disease

Research Interests: Investigating aberrant n-glycosylation through colorectal carcinoma progression.

Research Aims: My research focuses on elucidating the role of health disparities on altered N-glycosylation patterns in colorectal disease progression. Utilizing multimodal mass spectrometry imaging techniques, we aim to profile normal, pre-invasive lesions, adenomas, and CRC carcinoma tissue samples for facilitating translational applications and a deeper understanding of the intricate molecular landscape associated with disease progression

T32 ITOS Program

K12 Program Scholars

Barry Gibney, D.O.

Assistant Professor, Department of Surgery

Analysis of Mesothelioma Tumor Microenvironment Following Neoadjuvant Immunotherapy

Primary Mentor: John Wrangle, M.D.

Secondary Mentors: Shikhar Mehrotra, Ph.D., and Richard O'Neil, Ph.D.

Adam Fox, M.D.

Assistant Professor, Department of Medicine

Reflex Biomarker Testing to Increase Use of Targeted Therapies in Lung Cancer Proposed Didactic Course Of Study: Selected Courses

Primary Mentor: Gerard Silvestri, M.D.

Secondary Mentor: Paul Nietert, Ph.D.

K12 Scholars Program