Evidence map›Paper›PMID 31336613›Full record

ReviewInternational journal of molecular sciences2019

Biological Functions and Molecular Mechanisms of Antibiotic Tigecycline in the Treatment of Cancers.

Zhen Dong, Muhammad Nadeem Abbas, Saima Kausar, Jie Yang, Lin Li, Li Tan, Hongjuan Cui

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Targetable pathways for drug repurposing in gastric cancer.World journal of gastroenterology · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Drug Repurposing for Cancer Treatment: A Comprehensive Review.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
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  20. 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

7 authors at 1 institution in 1 country.

Zhen DongState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China.ORCID 0000-0003-3108-0245
Muhammad Nadeem AbbasState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China.
Saima KausarState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China.
Jie YangState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China.
Lin LiState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China.
Li TanState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China.
Hongjuan CuiState Key Laboratory of Silkworm Genome Biology, Institute of Sericulture and Systems Biology, Southwest University, Beibei, Chongqing 400716, China. hcui@swu.edu.cn.ORCID 0000-0003-1178-1570
Southwest University · CN

Funding

the Fundamental Research Funds for the Central Universities XDJK2019C013the National Key Research and Development Program of China No. 2016YFC1302204 and 2017YFC1308600the National Natural Science Foundation of China No. 81672502the Project Funded by Chongqing Special Postdoctoral Science Foundation No. XmT2018080
6 · The paper itself

Abstract

As an FDA-approved drug, glycylcycline tigecycline has been used to treat complicated microbial infections. However, recent studies in multiple hematologic and malignant solid tumors reveal that tigecycline treatment induces cell cycle arrest, apoptosis, autophagy and oxidative stress. In addition, tigecycline also inhibits mitochondrial oxidative phosphorylation, cell proliferation, migration, invasion and angiogenesis. Importantly, combinations of tigecycline with chemotherapeutic or targeted drugs such as venetoclax, doxorubicin, vincristine, paclitaxel, cisplatin, and imatinib, have shown to be promising strategies for cancer treatment. Mechanism of action studies reveal that tigecycline leads to the inhibition of mitochondrial translation possibly through interacting with mitochondrial ribosome. Meanwhile, this drug also interferes with several other cell pathways/targets including MYC, HIFs, PI3K/AKT or AMPK-mediated mTOR, cytoplasmic p21

Indexed as

AnimalsAnti-Bacterial AgentsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisAutophagyCell Cycle CheckpointsDrug RepositioningEnergy MetabolismGene Expression Regulation, NeoplasticHumansMitochondriaNeoplasmsSignal TransductionTigecyclineTreatment OutcomeAnti-Bacterial AgentsAntineoplastic AgentsTigecyclineantibioticsautophagycell cycle arrestmitochondrial translationOxPhostigecycline

Identifiers

PMID31336613
PMCPMC6678986
OpenAlexW2964273712

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.