Evidence map›Paper›PMID 31392076›Full record

ArticleAmerican journal of cancer research2019

Lenvatinib promotes antitumor immunity by enhancing the tumor infiltration and activation of NK cells.

Qing Zhang, Hongyan Liu, Hanhan Wang, Mengmeng Lu, Yangna Miao, Jiage Ding, Huizhong Li, Xiaoge Gao, Shishuo Sun, Junnian Zheng

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Lenvatinib enhances antitumor immunity of anti-PD-1 antibody.International journal of clinical oncology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. The potential of lenvatinib in breast cancer therapy.Medical oncology (Northwood, London, England) · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Article
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  15. Review
  16. Article
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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

10 authors at 1 institution in 1 country.

Qing ZhangCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Hongyan LiuCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Hanhan WangCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Mengmeng LuCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Yangna MiaoCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Jiage DingCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Huizhong LiCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Xiaoge GaoCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Shishuo SunCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Junnian ZhengCancer Institute, Xuzhou Medical University Xuzhou, Jiangsu, P. R. China.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based on previous reports, the efficacy of lenvatinib against cancer is mainly attributed to its antiangiogenic activity and its ability to suppress tumor proliferation, which are mediated by targeting receptor tyrosine kinases (RTKs). However, the effects of lenvatinib on tumor immune modulation have rarely been explored. Here, we show that lenvatinib effectively inhibited murine melanoma and renal cancer, and this inhibition was associated with enhanced tumor infiltration by natural killer (NK) cells. Critically, lenvatinib-induced tumor growth inhibition was attenuated by antibody-mediated NK cell depletion or the blockade of NK cell chemotaxis with an anti-CXCR3 blocking antibody. In addition, the expression of natural cytotoxicity receptors (NCRs) by tumor-infiltrating NK cells and the expression of cytotoxic cytokines in the tumor tissue were also augmented by lenvatinib. These data thus suggest that lenvatinib may be used not only as a direct cytotoxic drug against tumor angiogenesis and proliferation but also as a potent adjunct for enhancing the efficacy of immune-based cancer therapies by enhancing the tumor infiltration and activation of NK cells.

Indexed as

activationchemokineLenvatinibmelanomaNK cellrenal cancertumor infiltration

Identifiers

PMID31392076
PMCPMC6682710
OpenAlexW3022705128

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.