Evidence map›Paper›PMID 39297473›Full record

ArticleCurrent cancer drug targets2025

Dendrobine Suppresses Tumor Growth by Regulating the PD-1/PD-L1 Checkpoint Pathway in Lung Cancer.

Linmao Li, Jiejin Nong, Jingui Li, Lini Fang, Meini Pan, Haixian Qiu, Shiqing Huang, Yepeng Li, Meijuan Wei, Haiying Yin

Abstract read
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Article in Current cancer drug targets, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Research Progress on the Alkaloids ofCurrent issues in molecular biology · 2026
    Review
  2. Article
  3. Article
  4. 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

10 authors.

Linmao LiDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Jiejin NongDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Jingui LiDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Lini FangDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Meini PanDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Haixian QiuDepartment of Traditional Chinese Medicine, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Shiqing HuangDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Yepeng LiDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Meijuan WeiDepartment of Oncology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.
Haiying YinSchool of Nursing, Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, P.R. China.

Funding

Self-raised Project of Traditional Chinese Medicine in Guangxi Autonomous Region GXZYL20220303
6 · The paper itself

Abstract

backgroundDendrobine is a bioactive alkaloid isolated from Dendrobium nobile. Studies have evaluated the anti-tumor effect of dendrobine in cancers, including lung cancer. However, the mechanism of dendrobine inhibiting tumors requires further study.

methodsBioinformatics was performed to screen the potential targets of dendrobine. The intersection of dendrobine and lung cancer targets was performed for KEGG analysis. CCK-8 was used to detect cell viability after dendrobine treatment. A xenograft mouse model was established to explore the effect of dendrobine on lung cancer. The percentages of PD-L1+, CD4+, CD8+, CD11b+, CD25+FOXP3+ cells, the expression of Ki-67 and caspase-3, the expression of pathway-related proteins, the levels of IL-2, IFN-γ, and TGF-β, and the changes of indicators of liver and renal function were measured.

resultsDendrobine regulated the PD1/PD-L1 checkpoint signaling pathway and affected the occurrence and development of lung cancer. Dendrobine decreased the cell viability of lung cancer. Dendrobine and anti-PD-L1 decreased tumor growth, increased caspase-3 expression, and reduced Ki-67 expression in tumor tissues. Dendrobine and anti-PD-L1 suppressed protein expression of PD-L1, p-JAK1/JAK1, and p-JAK2/JAK2 in tumor tissues. Greatly, dendrobine and anti-PD-L1 decreased the percentages of PD-L1+, CD11b+, and CD25+FOXP3+ cells, increased the percentages of CD4+ and CD8+cells, and enhanced the levels of IL-2, IFN-γ, and TGF-β in tumor tissues. Dendrobine demonstrated no hepatorenal toxicity to the tumor mice. The combination of dendrobine and anti-PD-L1 greatly strengthened the effects of dendrobine on tumors.

conclusionDendrobine inhibited tumor immune escape by suppressing the PD-1/PD-L1 checkpoint pathway, thus restricting tumor growth of lung cancer.

Indexed as

AlkaloidsB7-H1 AntigenLung NeoplasmsProgrammed Cell Death 1 ReceptorAnimalsCell Line, TumorCell ProliferationHumansMiceMice, Inbred BALB CMice, NudeSignal TransductionXenograft Model Antitumor AssaysAlkaloidsB7-H1 AntigenCD274 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 ReceptorDendrobineimmunitylung cancerPD-L1tregstumor growth.

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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.