Evidence map›Paper›PMID 33750914›Full record

ArticleCommunications biology2021

Cell-autonomous immune gene expression is repressed in pulmonary neuroendocrine cells and small cell lung cancer.

Ling Cai, Hongyu Liu, Fang Huang, Junya Fujimoto, Luc Girard, Jun Chen, Yongwen Li, Yu-An Zhang, Dhruba Deb, Victor Stastny and 20 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 97 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Esophageal neuroendocrine carcinoma: molecular insights, diagnostic advances, and emerging treatment strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  5. Identification ofMolecular medicine reports · 2026
    Article
  6. iScience · 2026
    Article
  7. Article
  8. Review
  9. The Five-Decade Journey of Small Cell Lung Cancer.Cancer communications (London, England) · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. [Research Progress on the Role of Notch Signaling Pathway in Small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Current and future therapies for small cell lung carcinoma.Journal of hematology & oncology · 2025
    Review
  20. Article

2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 7 institutions in 2 countries.

Ling CaiQuantitative Biomedical Research Center, Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA. Ling.Cai@UTSouthwestern.edu.
Hongyu LiuQuantitative Biomedical Research Center, Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Fang HuangChildren's Research Institute, UT Southwestern Medical Center, Dallas, TX, USA.
Junya FujimotoDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Luc GirardSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Jun ChenTianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin Medical University General Hospital, Tianjin, China.
Yongwen LiTianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin Medical University General Hospital, Tianjin, China.ORCID 0000-0001-6102-2949
Yu-An ZhangHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX, USA.
Dhruba DebHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX, USA.
Victor StastnyHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX, USA.
Karine PozoDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Christin S KuoDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Gaoxiang JiaQuantitative Biomedical Research Center, Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Chendong YangChildren's Research Institute, UT Southwestern Medical Center, Dallas, TX, USA.
Wei ZouDepartment of Oncology Biomarker Development, Genentech Inc., South San Francisco, CA, USA.
Adeeb AlomarHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX, USA.
Kenneth HuffmanHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX, USA.
Mahboubeh Papari-ZareeiHamon Center for Therapeutic Oncology Research, UT Southwestern Medical Center, Dallas, TX, USA.
Lin YangDepartment of Pathology, National Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Benjamin DrapkinSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Esra A AkbayDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-4149-2529
David S ShamesDepartment of Oncology Biomarker Development, Genentech Inc., South San Francisco, CA, USA.
Ignacio I WistubaDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Tao WangQuantitative Biomedical Research Center, Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-4355-149X
Jane E JohnsonSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-8605-2746
Guanghua XiaoQuantitative Biomedical Research Center, Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
Ralph J DeBerardinisChildren's Research Institute, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-2705-7432
John D MinnaSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA. John.Minna@UTSouthwestern.edu.ORCID 0000-0002-7776-0767
Yang XieQuantitative Biomedical Research Center, Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, TX, USA. Yang.Xie@UTSouthwestern.edu.
Adi F GazdarSimmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Southwestern Medical Center · USTianjin Medical University General Hospital · CNThe University of Texas MD Anderson Cancer Center · USThe University of Texas Southwestern Medical Center · USChinese Academy of Medical Sciences & Peking Union Medical College · CNHoward Hughes Medical Institute · USStanford University · US

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Metabolic Regulators of Tumor Growth and ProgressionR35CA220449 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI RALPH J DEBERARDINIS · 2017 to 2026
$9.4M
Developing ASCL1 and NeuroD1 lineage oncogene targeted therapy for small cell lung cancerU01CA213338 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MINNA, JOHN D. · 2017 to 2021
$3.0M
Novel computational approaches to predict drug response and combination effectsR35GM136375 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI XIE, YANG · 2020 to 2024
$2.0M
Integrative Analysis to Identify Regulation Targets of RNA-Binding ProteinsR01GM115473 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI XIE, YANG · 2016 to 2019
$1.3M
NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA070907NCI NIH HHS R35 CA220449NCI NIH HHS U01 CA213338NIGMS NIH HHS R01 GM115473NIGMS NIH HHS R35 GM136375
6 · The paper itself

Abstract

Small cell lung cancer (SCLC) is classified as a high-grade neuroendocrine (NE) tumor, but a subset of SCLC has been termed "variant" due to the loss of NE characteristics. In this study, we computed NE scores for patient-derived SCLC cell lines and xenografts, as well as human tumors. We aligned NE properties with transcription factor-defined molecular subtypes. Then we investigated the different immune phenotypes associated with high and low NE scores. We found repression of immune response genes as a shared feature between classic SCLC and pulmonary neuroendocrine cells of the healthy lung. With loss of NE fate, variant SCLC tumors regain cell-autonomous immune gene expression and exhibit higher tumor-immune interactions. Pan-cancer analysis revealed this NE lineage-specific immune phenotype in other cancers. Additionally, we observed MHC I re-expression in SCLC upon development of chemoresistance. These findings may help guide the design of treatment regimens in SCLC.

Indexed as

TranscriptomeAnimalsAntineoplastic AgentsBiomarkers, TumorCell LineageCell Line, TumorDrug Resistance, NeoplasmGene Expression ProfilingGene Expression Regulation, NeoplasticGenes, MHC Class IHumansImmunophenotypingLung NeoplasmsMiceNeuroendocrine TumorsPhenotypeAntineoplastic AgentsBiomarkers, Tumor

Identifiers

PMID33750914
PMCPMC7943563
OpenAlexW3133593642

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.