Julia Qu

Associate Professor of Immunology and Immune Therapeutics

Image of Julia Qu
Is this your profile? Click to edit

Overview

The research in the Qu lab focuses on lung immunity, inflammation, and diseases, spanning acute injury, chronic conditions, infectious diseases, and lung cancer—the leading cause of cancer-related mortality worldwide. Using mouse and human co-clinical models and state-of-the-art technologies, the Qu group is trying to elucidate the cellular and molecular mechanisms underlying lung homeostasis and diseases development, progression, and therapy resistance, for preventive, prognostic, and therapeutic purposes, and is developing innovative therapies for lung cancer, the most devastating cancer type.

As the primary organ for gas exchange, the lung constantly encounters challenges from the external environment. The lung immune system, particularly the innate immunity, plays a crucial role in guarding the lung against these threats and maintaining lung homeostasis. The Qu research team is investigating the mechanisms underlying pulmonary immune regulation and its deregulation, particularly the innate immune components, in promoting lung inflammation and disease development and progression. At the cellular level, they mainly focus on lung epithelial cells and macrophages, the key sentinels in the lung and the main culprits of lung diseases. At the molecular level, they mainly focus on NF-κB and STAT signaling pathways, master regulators of cell survival, proliferation, and immunity.

Research Funding

  • The NF-kappaB modulator PDLIM2 as an intrinsic checkpoint of alveolar macrophages critical for lung innate immunity, inflammation and diseases
    NIH · R01HL177140 · Apr 1, 2025 – Jan 31, 2029 · Role: Principal Investigator
  • Mechanistic difference of NF-kappaB in lung physiology and tumorigenesis
    NIH · R01CA258614 · Aug 24, 2022 – Jul 31, 2027 · Role: Principal Investigator
  • Structural and molecular dissection of NF-kappaB regulation by the ubiquitin E3 ligase PDLIM2 in lung innate immunity and diseases
    NIH · R01GM144890 · Mar 10, 2022 – Feb 28, 2026 · Role: Principal Investigator
  • Clinicopathological significance of PDLIM2 in HIV/AIDS-related malignancies caused by KSHV
    NIH · R21CA189703 · Jul 1, 2015 – Jun 30, 2018 · Role: Principal Investigator

Publications

  • PDLIM2 in lung adenocarcinoma metastasis. Neoplasia. 2026 Sep 25; 81:101371.. View in PubMed
  • Exploring PDLIM2 as a prognostic biomarker and therapeutic target in lung adenocarcinoma. Br J Cancer. 2026 Aug 08.. View in PubMed
  • An Advanced Single-Cell RNA Sequencing (scRNA-seq) Protocol Utilizing Custom-Designed Multiplexing. Bio Protoc. 2026 May 05; 16(9):e5678.. View in PubMed
  • AKT Signaling Differentially Regulates the Expression of Two Evolutionarily Conserved Wnt5a Isoforms in Lung Mesenchymal Cells. Cells. 2026 May 04; 15(9).. View in PubMed
  • PDLIM2 repression: a common mechanism in viral lung infection. Immunohorizons. 2026 Mar 10; 10(3).. View in PubMed
  • Alveolar epithelial NF-κB/RelA guards the lung against bacterial infection. J Immunol. 2026 Feb 09; 215(2).. View in PubMed
  • PDLIM2 in Lung Adenocarcinoma Metastasis. bioRxiv. 2025 Dec 07.. View in PubMed
  • SRC at the crossroads of KRAS inhibitor resistance: Mechanisms and therapeutic opportunities. Cancer Lett. 2026 Feb 28; 639:218194.. View in PubMed
  • Myeloid PDLIM2 repression as a common mechanism of infection susceptibility in lung diseases. Front Immunol. 2025; 16:1669117.. View in PubMed
  • PDLIM2 Repression: A Common Mechanism in Viral Lung Infection. bioRxiv. 2025 Sep 17.. View in PubMed