Evidence map›Paper›PMID 31871166›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Immunity against cancer cells may promote their proliferation and metastasis.

Chih-Wei Lin, Jia Xie, Ding Zhang, Kyung Ho Han, Geramie Grande, Nicholas C Wu, Zhuo Yang, Kyungmoo Yea, Richard A Lerner

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Technologies for Monoclonal Antibody Discovery and Development.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Phytogalactolipids activate humoral immunity against colorectal cancer.Journal of experimental & clinical cancer research : CR · 2023
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
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

9 authors at 2 institutions in 2 countries.

Chih-Wei LinDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037.
Jia XieDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037.
Ding ZhangDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037.
Kyung Ho HanDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037.ORCID 0000-0001-6907-1462
Geramie GrandeDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037.
Nicholas C WuDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037.
Zhuo YangDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037.
Kyungmoo YeaDepartment of New Biology, DGIST (Daegu Gyeongbuk Institute of Science and Technology), 42988 Daegu, Republic of Korea.
Richard A LernerDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037; rlerner@scripps.edu.
Scripps Research Institute · USDaegu Gyeongbuk Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein we present a concept in cancer where an immune response is detrimental rather than helpful. In the cancer setting, the immune system is generally considered to be helpful in curtailing the initiation and progression of tumors. In this work we show that a patient's immune response to their tumor can, in fact, either enhance or inhibit tumor cell growth. Two closely related autoantibodies to the growth factor receptor TrkB were isolated from cancer patients' B cells. Although highly similar in sequence, one antibody was an agonist while the other was an antagonist. The agonist antibody was shown to increase breast cancer cell growth both in vitro and in vivo, whereas the antagonist antibody inhibited growth. From a mechanistic point of view, we showed that binding of the agonist antibody to the TrkB receptor was functional in that it initiated downstream signaling identical to its natural growth factor ligand, brain-derived neurotrophic factor (BDNF). Our study shows that individual autoantibodies may play a role in cancer patients.

Indexed as

AnimalsAutoantibodiesAutoantigensB-LymphocytesBrain-Derived Neurotrophic FactorBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationFemaleHumansMembrane GlycoproteinsMiceNeoplasm MetastasisReceptor, trkBSignal TransductionAutoantibodiesAutoantigensBDNF protein, humanBrain-Derived Neurotrophic FactorMembrane GlycoproteinsReceptor, trkBtropomyosin-related kinase-B, humanagonistantibodycancer

Identifiers

PMID31871166
PMCPMC6955299
OpenAlexW2998272253

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.