Xiaotong Li

ORCID: 0000-0003-1644-6835
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Cancer Genomics and Diagnostics
  • Cancer Immunotherapy and Biomarkers
  • Cancer-related molecular mechanisms research
  • Nonmelanoma Skin Cancer Studies
  • Genetic factors in colorectal cancer
  • RNA modifications and cancer
  • Genomics and Chromatin Dynamics
  • Atherosclerosis and Cardiovascular Diseases
  • Head and Neck Cancer Studies
  • Breast Cancer Treatment Studies
  • MicroRNA in disease regulation
  • Evolution and Genetic Dynamics
  • Bioinformatics and Genomic Networks
  • BRCA gene mutations in cancer
  • Nutrition, Genetics, and Disease
  • Dental Implant Techniques and Outcomes
  • RNA Research and Splicing
  • Immunotherapy and Immune Responses
  • Genomics and Phylogenetic Studies
  • Lung Cancer Treatments and Mutations
  • dental development and anomalies
  • Orthodontics and Dentofacial Orthopedics
  • Epigenetics and DNA Methylation
  • Cancer, Hypoxia, and Metabolism
  • Gene expression and cancer classification

Zhejiang University
2025

China Pharmaceutical University
2020-2025

Capital Medical University
2023-2025

Shanxi Medical University
2024

Institute of Basic Medical Sciences of the Chinese Academy of Medical Sciences
2024

Beijing Institute of Education
2024

Beijing Tian Tan Hospital
2024

Yale University
2018-2023

Yale Cancer Center
2018-2023

Academy of Military Medical Sciences
2023

Joana Carlevaro-Fita Andrés Lanzós Lars Feuerbach Chen Hong David Mas-Ponte and 95 more Jakob Skou Pedersen Federico Abascal Samirkumar B. Amin Gary D. Bader Jonathan Barenboim Rameen Beroukhim Johanna Bertl Keith A. Boroevich Søren Brunak Peter J. Campbell Joana Carlevaro-Fita Dimple Chakravarty Calvin Wing Yiu Chan Ken Chen Jung Kyoon Choi Jordi Deu-Pons Priyanka Dhingra Klev Diamanti Lars Feuerbach J. Lynn Fink Nuno A. Fonseca Joan Frigola Carlo Gambacorti‐Passerini Dale W. Garsed Mark Gerstein Gad Getz Abel González-Pérez Qianyun Guo Marta Gut David Haan Mark P. Hamilton Nicholas J. Haradhvala Arif Harmanci Mohamed Helmy Carl Herrmann Julian M. Hess Asger Hobolth Ermin Hodzic Chen Hong Henrik Hornshøj Keren Isaev José M. G. Izarzugaza Rory Johnson Todd A. Johnson Malene Juul Randi Istrup Juul André Kahles Abdullah Kahraman Manolis Kellis Ekta Khurana Seungchan Kim Jong K. Kim Young-Wook Kim Jan Komorowski Jan O. Korbel Sushant Kumar Andrés Lanzós Erik G. Larsson Michael S. Lawrence Dong-Hoon Lee Kjong-Van Lehmann Shantao Li Xiaotong Li Ziao Lin Eric Minwei Liu Lucas Lochovsky Shaoke Lou Tobias Madsen Kathleen Marchal Iñigo Martincorena Alexander Martinez‐Fundichely Yosef E. Maruvka Patrick D. McGillivray Matthew Meyerson Ferran Muiños Loris Mularoni Hidewaki Nakagawa Morten Muhlig Nielsen Marta Paczkowska Keunchil Park Kiejung Park Jakob Skou Pedersen Oriol Pich Tirso Pons Sergio Pulido-Tamayo Benjamin J. Raphael Jüri Reimand Iker Reyes-Salazar Matthew A. Reyna Esther Rheinbay Mark A. Rubin Carlota Rubio-Pérez Radhakrishnan Sabarinathan S. Cenk Sahinalp Gordon Saksena

Abstract Long non-coding RNAs (lncRNAs) are a growing focus of cancer genomics studies, creating the need for resource lncRNAs with validated roles. Furthermore, it remains debated whether mutated can drive tumorigenesis, and such functions could be conserved during evolution. Here, as part ICGC/TCGA Pan-Cancer Analysis Whole Genomes (PCAWG) Consortium, we introduce Cancer LncRNA Census (CLC), compilation 122 GENCODE causal roles in phenotypes. In contrast to existing databases, CLC requires...

10.1038/s42003-019-0741-7 article EN cc-by Communications Biology 2020-02-05
Marta Paczkowska Jonathan Barenboim Nardnisa Sintupisut Natalie S. Fox Helen Zhu and 95 more Diala Abd-Rabbo Miles W. Mee Paul C. Boutros Federico Abascal Samirkumar B. Amin Gary D. Bader Rameen Beroukhim Johanna Bertl Keith A. Boroevich Søren Brunak Peter J. Campbell Joana Carlevaro-Fita Dimple Chakravarty Calvin Wing Yiu Chan Ken Chen Jung Kyoon Choi Jordi Deu-Pons Priyanka Dhingra Klev Diamanti Lars Feuerbach J. Lynn Fink Nuno A. Fonseca Joan Frigola Carlo Gambacorti‐Passerini Dale W. Garsed Mark Gerstein Gad Getz Abel González-Pérez Qianyun Guo Marta Gut David Haan Mark Hamilton Nicholas J. Haradhvala Arif Harmanci Mohamed Helmy Carl Herrmann Julian M. Hess Asger Hobolth Ermin Hodzic Chen Hong Henrik Hornshøj Keren Isaev José M. G. Izarzugaza Rory Johnson Todd A. Johnson Malene Juul Randi Istrup Juul André Kahles Abdullah Kahraman Manolis Kellis Ekta Khurana Jaegil Kim Jong K. Kim Young-Wook Kim Jan Komorowski Jan O. Korbel Sushant Kumar Andrés Lanzós Michael S. Lawrence Dong-Hoon Lee Kjong-Van Lehmann Shantao Li Xiaotong Li Ziao Lin Eric Minwei Liu Lucas Lochovsky Shaoke Lou Tobias Madsen Kathleen Marchal Iñigo Martincorena Alexander Martinez‐Fundichely Yosef E. Maruvka Patrick D. McGillivray William Meyerson Ferran Muiños Loris Mularoni Hidewaki Nakagawa Morten Muhlig Nielsen Keunchil Park Kiejung Park Jakob Skou Pedersen Oriol Pich Tirso Pons Sergio Pulido-Tamayo Benjamin J. Raphael Iker Reyes-Salazar Matthew A. Reyna Esther Rheinbay Mark A. Rubin Carlota Rubio-Pérez Radhakrishnan Sabarinathan S. Cenk Şahinalp Gordon Saksena Leonidas Salichos Chris Sander

Multi-omics datasets represent distinct aspects of the central dogma molecular biology. Such high-dimensional profiles pose challenges to data interpretation and hypothesis generation. ActivePathways is an integrative method that discovers significantly enriched pathways across multiple using statistical fusion, rationalizes contributing evidence highlights associated genes. As part ICGC/TCGA Pan-Cancer Analysis Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing from...

10.1038/s41467-019-13983-9 article EN cc-by Nature Communications 2020-02-05

Abstract ENCODE comprises thousands of functional genomics datasets, and the encyclopedia covers hundreds cell types, providing a universal annotation for genome interpretation. However, particular applications, it may be advantageous to use customized annotation. Here, we develop such custom by leveraging advanced assays, as eCLIP, Hi-C, whole-genome STARR-seq on number data-rich types. A key aspect this is comprehensive experimentally derived networks both transcription factors RNA-binding...

10.1038/s41467-020-14743-w article EN cc-by Nature Communications 2020-07-29
Matthew A. Reyna David Haan Marta Paczkowska Lieven P. C. Verbeke Miguél Vázquez and 95 more Abdullah Kahraman Sergio Pulido-Tamayo Jonathan Barenboim Lina Wadi Priyanka Dhingra Raunak Shrestha Gad Getz Michael S. Lawrence Jakob Skou Pedersen Mark A. Rubin David A. Wheeler Søren Brunak José M. G. Izarzugaza Ekta Khurana Kathleen Marchal Christian von Mering S. Cenk Şahinalp Alfonso Valencia Federico Abascal Samirkumar B. Amin Gary D. Bader Pratiti Bandopadhayay Rameen Beroukhim Johanna Bertl Keith A. Boroevich John Busanovich Peter J. Campbell Joana Carlevaro-Fita Dimple Chakravarty Calvin Wing Yiu Chan Ken Chen Jung Kyoon Choi Jordi Deu-Pons Klev Diamanti Lars Feuerbach J. Lynn Fink Nuno A. Fonseca Joan Frigola Carlo Gambacorti‐Passerini Dale W. Garsed Mark Gerstein Qianyun Guo Marta Gut Mark P. Hamilton Nicholas J. Haradhvala Arif Harmanci Mohamed Helmy Carl Herrmann Julian M. Hess Asger Hobolth Ermin Hodzic Chen Hong Henrik Hornshøj Keren Isaev Rory Johnson Todd A. Johnson Malene Juul Randi Istrup Juul André Kahles Manolis Kellis Seungchan Kim Jong K. Kim Young-Wook Kim Jan Komorowski Jan O. Korbel Sushant Kumar Andrés Lanzós Erik Larsson Donghoon Lee Kjong-Van Lehmann Shantao Li Xiaotong Li Ziao Lin Eric Minwei Liu Lucas Lochovsky Shaoke Lou Tobias Madsen Iñigo Martincorena Alexander Martinez‐Fundichely Yosef E. Maruvka Patrick D. McGillivray William Meyerson Ferran Muiños Loris Mularoni Hidewaki Nakagawa Morten Muhlig Nielsen Keunchil Park Kiejung Park Tirso Pons Iker Reyes-Salazar Esther Rheinbay Carlota Rubio-Pérez Gordon Saksena Leonidas Salichos Chris Sander

Abstract The catalog of cancer driver mutations in protein-coding genes has greatly expanded the past decade. However, non-coding are less well-characterized and only a handful recurrent mutations, most notably TERT promoter have been reported. Here, as part ICGC/TCGA Pan-Cancer Analysis Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2658 across 38 tumor types, we perform multi-faceted pathway network analyses 2583 genomes 27 types compiled by PCAWG...

10.1038/s41467-020-14367-0 article EN cc-by Nature Communications 2020-02-05

Multi-region sequencing is used to detect intratumor genetic heterogeneity (ITGH) in tumors. To assess whether genuine ITGH can be distinguished from artifacts, we performed whole-exome (WES) on three anatomically distinct regions of the same tumor with technical replicates estimate noise. Somatic variants were detected different WES pipelines and subsequently validated by high-depth amplicon sequencing. The cancer-only pipeline was unreliable, about 69% identified somatic being false...

10.1016/j.celrep.2018.10.046 article EN cc-by Cell Reports 2018-11-01

How the immune microenvironment changes during neoadjuvant chemotherapy of primary breast cancer is not well understood.We analyzed pre- and post-treatment samples from 60 patients using NanoString PanCancer IO360™ assay to measure expression 750 immune-related genes corresponding 14 cell types various functions, assessed TIL counts PD-L1 protein by immunohistochemistry. Treatment associated in gene levels were compared t-test with Bonferroni correction. count, metagenes Wilcoxon test....

10.1186/s40425-019-0563-7 article EN cc-by Journal for ImmunoTherapy of Cancer 2019-04-09

Neural stem cells (NSCs) are critical for brain development and maintenance of neurogenesis. However, the molecular mechanisms that regulate NSC proliferation differentiation remain unclear. Mysm1 is a deubiquitinase essential self-renewal several cells. It unknown whether plays an important role in NSCs. Here, we found was expressed NSCs its expression increased with age mice. Mice knockdown by crossing floxed mice Nestin-Cre exhibited abnormal microcephaly. deletion promoted apoptosis,...

10.1038/s41419-024-06530-y article EN cc-by Cell Death and Disease 2024-02-12
Shimin Shuai Federico Abascal Samirkumar B. Amin Gary D. Bader Pratiti Bandopadhayay and 95 more Jonathan Barenboim Rameen Beroukhim Johanna Bertl Keith A. Boroevich Søren Brunak Peter J. Campbell Joana Carlevaro-Fita Dimple Chakravarty Calvin Wing Yiu Chan Ken Chen Jung Kyoon Choi Jordi Deu-Pons Priyanka Dhingra Klev Diamanti Lars Feuerbach J. Lynn Fink Nuno A. Fonseca Joan Frigola Carlo Gambacorti‐Passerini Dale W. Garsed Mark Gerstein Gad Getz Qianyun Guo Marta Gut David Haan Mark P. Hamilton Nicholas J. Haradhvala Arif O. Harmanci Mohamed Helmy Carl Herrmann Julian M. Hess Asger Hobolth Ermin Hodzic Hong Chen Henrik Hornshøj Keren Isaev José M. G. Izarzugaza Rory Johnson Todd A. Johnson Malene Juul Randi Istrup Juul André Kahles Abdullah Kahraman Manolis Kellis Ekta Khurana Jaegil Kim Jong-Kwang Kim Young-Wook Kim Jan Komorowski Jan O. Korbel Sushant Kumar Andrés Lanzós Erik G. Larsson Michael S. Lawrence Donghoon Lee Kjong-Van Lehmann Shantao Li Xiaotong Li Ziao Lin Eric Minwei Liu Lucas Lochovsky Shaoke Lou Tobias Madsen Kathleen Marchal Iñigo Martincorena Alexander Martinez‐Fundichely Yosef E. Maruvka Patrick D. McGillivray Matthew Meyerson Ferran Muiños Loris Mularoni Hidewaki Nakagawa Morten Muhlig Nielsen Marta Paczkowska Keunchil Park Kiejung Park Jakob Skou Pedersen Tirso Pons Sergio Pulido-Tamayo Benjamin J. Raphael Jüri Reimand Iker Reyes-Salazar Matthew A. Reyna Esther Rheinbay Mark A. Rubin Carlota Rubio-Pérez S. Cenk Şahinalp Gordon Saksena Leonidas Salichos Chris Sander Steven E. Schumacher Mark Shackleton Ofer Shapira Ciyue Shen Raunak Shrestha

Abstract The discovery of driver mutations is one the key motivations for cancer genome sequencing. Here , as part ICGC/TCGA Pan-Cancer Analysis Whole Genomes (PCAWG) Consortium which aggregated whole sequencing data from 2658 cancers across 38 tumour types, we describe DriverPower, a software package that uses mutational burden and functional impact evidence to identify in coding non-coding sites within genomes. Using total 1373 genomic features derived public sources, DriverPower’s...

10.1038/s41467-019-13929-1 article EN cc-by Nature Communications 2020-02-05

Reprogramming of glucose metabolism is a key event in tumorigenesis and progression. Here, we show that active c-Src stimulates glycolysis by phosphorylating (Tyr194) activating PFKFB3, enzyme boosts producing fructose-2,6-bisphosphate PFK1. Increased intermediates replenish non-oxidative pentose phosphate pathway (PPP) serine for biosynthesis cancer cells. PFKFB3 knockout (KO) cells their counterpart reconstituted with PFKFB3-Y194F comparably impaired abilities proliferation, migration,...

10.1016/j.celrep.2020.03.005 article EN cc-by-nc-nd Cell Reports 2020-03-01

A precise predictive biomarker for TNBC response to immunochemotherapy is urgently needed. We previously established a 27-gene IO signature derived from 101-gene model classifying TNBC. Here we report pilot study assess the performance of in predicting pCR preoperative immunochemotherapy. obtained RNA sequencing data primary tumors 55 patients with TNBC, who received neoadjuvant PD-L1 blocker durvalumab. determined power and accuracy immunomodulatory (IM) subtype identified by model,...

10.3390/cancers13194839 article EN Cancers 2021-09-28

Abstract Purpose: We examined gene expression, germline variant, and somatic mutation features associated with pathologic response to neoadjuvant durvalumab plus chemotherapy in basal-like triple-negative breast cancer (bTNBC). Experimental Design: Germline whole-exome DNA RNA sequencing, programmed death ligand 1 (PD-L1) IHC, stromal tumor-infiltrating lymphocyte scoring were performed on 57 patients. validated our results using 162 patients from the GeparNuevo randomized trial. Results:...

10.1158/1078-0432.ccr-21-3215 article EN Clinical Cancer Research 2022-04-04

Temporal predictive models have the potential to improve decisions in health care, public services, and other domains, yet they often fail effectively support decision-makers. Prior literature shows that many misalignments between model behavior decision-makers' expectations stem from issues of specification, namely how, when, for whom predictions are made. However, specifications tasks highly technical difficult non-data-scientist stakeholders interpret critique. To address this challenge...

10.1145/3706598.3713664 preprint EN arXiv (Cornell University) 2025-02-14

Background Research data regarding the correlation between elevated oxidised low-density lipoprotein (oxLDL) cholesterol concentrations and unfavourable clinical outcomes in individuals experiencing minor acute ischaemic cerebrovascular events or transient attack (TIA) with presumed atherosclerotic aetiology are still limited. Methods This investigation incorporated a cohort of 5814 participants derived from Intensive Statin Antiplatelet Therapy for Acute High-Risk Intracranial Extracranial...

10.1136/svn-2024-003664 article EN cc-by-nc-nd Stroke and Vascular Neurology 2025-02-26

We previously reported that p38 MAPK signaling is required for osteoclast differentiation but not function. Here we further investigated the role of in function and mouse bone marrow macrophages (BMM phi), common precursors osteoclasts dendritic cells. Lipopolysaccharide (LPS) activated pathway BMM phi by sequential phosphorylation kinase 3/6, MAPK, activating transcription factor-2. Treatment with SB203580, a inhibitor, suppressed LPS-induced LPS stimulated production IL-1 beta, TNF alpha,...

10.1210/en.2003-0166 article EN Endocrinology 2003-07-29

// Qi Liu 1 , Zhen Cheng Lianzhong Luo 2 Yun Yang 3 Zhenzhu Zhang Huanhuan Ma Tao Chen Xi Huang Shu-Yong Lin Meijun Jin Qinxi Li Xiaotong State Key Laboratory for Cellular Stress Biology, School of Life Sciences, Xiamen University, Fujian 361102, China Central Laboratory, Medical College, Xiamen, 361008, Basic Xinxiang Henan 453003, Correspondence to: Li, e-mail: xtli@xmu.edu.cn liqinxi@xmu.edu.cn Keywords: MUC16, C-terminus, β-catenin, Wnt signaling, tumorigenesis Received: December 09,...

10.18632/oncotarget.9191 article EN Oncotarget 2016-05-05

Salinity is a critical abiotic stress, which significantly impacts the agricultural yield worldwide. Identification of molecular mechanisms underlying salt tolerance in euhalophyte Suaeda salsa conducive to development salt-resistant crops. In present study, high-throughput RNA sequencing was performed after S. leaves were exposed 300 mM NaCl for 7 days, and 7,753 unigenes identified as differently expressed genes (DEGs) salsa, including 3,638 increased 4,115 decreased unigenes. Moreover,...

10.1038/s41598-020-61204-x article EN cc-by Scientific Reports 2020-03-06

Sequence variations in coding and non-coding regions of the genome can affect gene expression signalling pathways, which turn may influence disease outcome. In this study, we integrated somatic mutations, clinical data from 930 breast cancer patients included TCGA database. Genes associated with single mutations molecular subtypes were identified by Mann-Whitney U-test their prognostic value was evaluated Kaplan-Meier Cox regression analyses. Results confirmed using profiles Metabric set (n...

10.1038/s41416-018-0030-0 article EN cc-by British Journal of Cancer 2018-03-21

Two hallmarks of cancer cells are their resistance to apoptosis and ability thrive despite reduced levels vital serum components. c-jun N-terminal kinase (JNK) activation is crucial for triggered by starvation (SS), isocitrate dehydrogenase 1 (IDH1) mutations tumorigenic, in part, because they produce the abnormal metabolite 2-hydroxyglutarate (2-HG). However, it unknown whether 2-HG-induced tumorigenesis partially due JNK inhibition thus defective SS-induced apoptosis. We show here, using...

10.1016/j.celrep.2017.03.053 article EN cc-by-nc-nd Cell Reports 2017-04-01

Murine MARCO has been identified recently in subsets of macrophages located the peritoneum, marginal zone spleen, and medullary cord lymph nodes, where it proposed that serves as a bacteria‐binding receptor. A scavenger receptor family member with an extended collagenous domain, murine also demonstrated atherosclerotic lesions susceptible mice. We report here identification, tissue chromosomal localization, pharmacological characterization human (h)MARCO. hMARCO was from macrophage cDNA...

10.1046/j.1432-1327.2000.01077.x article EN European Journal of Biochemistry 2000-02-01

The human checkpoint kinase 2 (Chk2) plays a central role in regulation of the cellular response to DNA damage, resulting cell cycle arrest, repair, or apoptosis depending on severity damage and context. Chk2 inhibitors are being developed as sensitizers for chemotherapeutic agents. In contrast, here we report that direct activation alone (without agents) led potent inhibition cancer proliferation. absence de novo was achieved by increased expression, evidenced its phosphorylation at Thr68,...

10.1158/0008-5472.can-05-0677 article EN Cancer Research 2005-07-15

EP300-interacting inhibitor of differentiation 1 (EID1) belongs to a protein family implicated in the control transcription, differentiation, DNA repair, and chromosomal maintenance. EID1 has very short half-life, especially G0 cells. We discovered that contains peptidic, modular degron is necessary sufficient for its polyubiquitylation proteasomal degradation. found this recognized by an Skp1, Cullin, F-box (SCF)-containing ubiquitin ligase complex uses Only Protein 21 (FBXO21) as substrate...

10.1073/pnas.1522006112 article EN Proceedings of the National Academy of Sciences 2015-12-02
Coming Soon ...