The Quelle Lab Mission

The Quelle research program investigates druggable mechanisms driving cancer with an emphasis on cell cycle and mitogenic signaling pathways (e.g., CDKs, RB1, ARF, p53, AKT, etc). Our funded efforts currently explore the pathogenesis of two very different cancers – slowly growing neuroendocrine tumors (NETs) and aggressive malignant peripheral nerve sheath tumors (MPNSTs). NET patients generally live a long time following diagnosis due to the indolent nature of the disease, but more effective therapies are desperately needed once tumors become resistant to current treatments. By comparison, MPNSTs are deadly sarcomas in both children and adults, and sadly, there are no effective therapies for these patients.

 

In our studies, we employ various model systems including cultured cells (normal and tumor-derived), mouse and pig cancer models, and human tumor specimens. Our research is interdisciplinary and collaborative, routinely involving interactions with other basic scientists and clinical colleagues as well as biostatisticians. Our goal is to perform meaningful and innovative translational oncology that will improve therapies for cancer patients.

 

Recent Publications

  • Lingo JJ, Reis R, Koyas A, Voigt E, Zacharias ZR, Allamargot C, Hornick EL, Raygoza Garay JA, Kaemmer CA, Elias EC, Jabbari A, Wilhelm CR, Boyden AW, Karandikar NJ, Breheny P, Meyerholz DK, Dodd RD, Houtman JCD, Darbro BW, Quelle DE. Intratumoral plasma cells mediate a pro-inflammatory response to kinase inhibition and successful immune checkpoint blockade therapy in malignant peripheral nerve sheath tumours. EBioMedicine 131:106413, 2026. DOI: 10.1016/j.ebiom.2026.106413. PMID: 42541926. PMCID: PMC13453594
  • Voigt EM, Isaacson AL, Leidinger MR, Goeken JA, Hanigan Q, Guo DF, Gasser RM, Eadie M, Babor I, Darbro BW, Paradee W, Rahmouni K, Zhao T, Breheny P, Lee E, Kim M, Meyerholz DK, Milhem M, Dodd RD, Quelle DE. Development of a Cre-inducible Rabl6a transgenic mouse model that enhances sarcoma growth in vivo. Cancers 18(14):2230, 2026. DOI: 10.3390/cancers18142230. PMID: 42512296. PMCID: PMC13407154
  • Kohlmeyer JL, Lingo JJ, Kaemmer CA, Scherer A, Warrier A, Voigt E, Raygoza Garay JA, McGivney GR, Brockman QR, Tang A, Calizo A, Pollard K, Zhang X, Hirbe AC, Pratilas CA, Leidinger M, Breheny P, Chimenti MS, Sieren JC, Monga V, Tanas MR, Meyerholz DK, Darbro BW, Dodd RD, Quelle DE. CDK4/6-MEK inhibition in MPNSTs causes plasma cell infiltration, sensitization to PD-L1 blockade, and tumor regression. Clin Cancer Res. 2023 Jul 6:CCR-23-0749. doi: 10.1158/1078-0432.CCR-23-0749. Online ahead of print. PMID: 37410426
All Publications

See Dr. Quelle's complete list of publications on PubMed.