
Xin Gao
· Assistant Professor (Wisconsin Blood Cancer Research Institute)University of Wisconsin-Madison · Pathology and Laboratory Medicine
Active 1996–2025
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About
Xin Gao, PhD, is an Assistant Professor who obtained her PhD from the University of Wisconsin-Madison in 2016, working in Emery Bresnick’s lab. Following her doctoral studies, she completed two postdoctoral fellowships: one at Albert Einstein College of Medicine in Paul Frenette's lab, and another at UW-Madison in Jing Zhang's lab. Dr. Gao has been recognized with a K01 award and the ASH Fellow-to-Faculty Scholar Award, which have supported her research focusing on the bone marrow microenvironment and hematopoietic stem cells. She joined the faculty at UW-Madison in 2023.
Research topics
- Biology
- Immunology
- Cancer research
- Genetics
- Cell biology
Selected publications
Blood · 2021 · 56 citations
Mutations in chromatin regulator ASXL1 are frequently identified in myeloid malignancies, in particular ∼40% of patients with chronic myelomonocytic leukemia (CMML). ASXL1 mutations are associated with poor prognosis in CMML and significantly co-occur with NRAS mutations. Here, we show that concurrent ASXL1 and NRAS mutations defined a population of CMML patients who had shorter leukemia-free survival than those with ASXL1 mutation only. Corroborating this human data, Asxl1-/- accelerated CMML p…
Journal of Clinical Investigation · 2023-10-17 · 14 citations
articleOpen accessWe previously demonstrated that a subset of acute myeloid leukemia (AML) patients with concurrent RAS pathway and TP53 mutations have an extremely poor prognosis and that most of these TP53 mutations are missense mutations. Here, we report that, in contrast to the mixed AML and T cell malignancy that developed in NrasG12D/+ p53-/- (NP-/-) mice, NrasG12D/+ p53R172H/+ (NPmut) mice rapidly developed inflammation-associated AML. Under the inflammatory conditions, NPmut hematopoietic stem and progeni…
2024-09-03
preprintOpen access<div>AbstractPurpose:<p>In multiple myeloma (MM), therapy-induced clonal evolution is associated with treatment resistance and is one of the most important hindrances toward a cure for MM. To further understand the molecular mechanisms controlling the clonal evolution of MM, we applied single-cell RNA sequencing (scRNA-seq) to paired diagnostic and posttreatment bone marrow (BM) samples.</p>Experimental Design:<p>scRNA-seq was performed on 38 BM samples from patients with…
2024-09-03
preprintOpen access<div>AbstractPurpose:<p>In multiple myeloma (MM), therapy-induced clonal evolution is associated with treatment resistance and is one of the most important hindrances toward a cure for MM. To further understand the molecular mechanisms controlling the clonal evolution of MM, we applied single-cell RNA sequencing (scRNA-seq) to paired diagnostic and posttreatment bone marrow (BM) samples.</p>Experimental Design:<p>scRNA-seq was performed on 38 BM samples from patients with…
2024-09-03
preprintOpen access<p>Supplemental table 1-15.</p>
Frequent coauthors
- 61 shared
Shaoshan Hu
Harbin Medical University
- 56 shared
Hang Ji
Sichuan University
- 53 shared
Emery H. Bresnick
University of Wisconsin Carbone Cancer Center
- 46 shared
Jiheng Zhang
Harbin Medical University
- 46 shared
Jianyang Du
Zhejiang Provincial People's Hospital
- 45 shared
Kirby D. Johnson
University of Wisconsin Carbone Cancer Center
- 45 shared
Zhihui Liu
Liaoning Provincial People's Hospital
- 42 shared
Nan Wang
Minzu University of China
Labs
Gao LabPI
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