Evidence map›Paper›PMID 34151717›Full record

ArticleBioengineered2021

Impact of Bupivacaine on malignant proliferation, apoptosis and autophagy of human colorectal cancer SW480 cells through regulating NF-κB signaling path.

Bingwu Liu, Xinfeng Yan, Zuojia Hou, Lei Zhang, Duwen Zhang

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. An End-to-endProceedings. IEEE International Conference on Healthcare Informatics · 2023
    Article
  8. Review
  9. Discovery of New Triterpenoids Extracted fromAntioxidants (Basel, Switzerland) · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Article
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

5 authors at 4 institutions in 1 country.

Bingwu LiuDepartment of Anesthesiology, The Second Children and Women's Healthcare of Jinan City, Jinan City, Shandong Province, China.
Xinfeng YanDepartment of Anesthesiology, The Second Children and Women's Healthcare of Jinan City, Jinan City, Shandong Province, China.
Zuojia HouDepartment of Anesthesiology, Laiwu People's Hospital of Jinan City, Jinan City, Shandong Province, China.
Lei ZhangDepartment of Anesthesiology, Laiwu Iron and Steel Group Laiwu Mining Co., Ltd. Staff Hospital, Jinan City, Shandong Province, China.
Duwen ZhangDepartment of Anesthesiology, Guizhou Provincial People's Hospital, Guiyang City, Guizhou Province, China.
Jinan Maternity And Care Hospital · CNGuizhou Provincial People's Hospital · CNJinan City People's Hospital · CNShandong Iron and Steel Group (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To probe into the impact of Bupivacaine on colorectal cancer (CRC) proliferation, apoptosis, and autophagy through regulating the NF-κB signaling pathway. Our work treated CRC cells with Bupivacaine, detected cell vitality through MTT assay, apoptosis through flow cytometry, cell migration through wound healing assay, NF-κB activity through immunofluorescence, inflammatory factor level, including TNF-α, IL-1β as well as IL-6 through ESLIA, apoptosis factor mRNA expression, including Bcl-2, Bax and caspase-3q through qRT-PCR, and protein expression linking with NF-κB signaling pathway as well as autophagy-related proteins via western blot. In in vivo experiments, we explored the impact of Bupivacaine on tumor volume, tumor and NF-κB expression. The results showed that 1 mM Bupivacaine was available to signally inhibit CRC cell vitality, promoted apoptosis rate and apoptosis gene expression, like Bax, and caspase-3, inhibited Bcl-2 expression, inhibited cancer cell migration, promoted autophagy-related protein LC3B II/LC3B I ratio and beclin-1 expression, and inhibited p62 expression. Additionally, it could elevate inflammatory factor level and induce IKK and IκB phosphorylation as well as NF-κB proteins. In in vivo experiments, Bupivacaine inhibited tumor volume and tumor, as well as NF-κB expression. In short, bupivacaine is available to inhibit CRC proliferation through regulating NF-κB signaling pathway, promote apoptosis and autophagy, and can be used as a potential drug to treat CRC in the future.

Indexed as

AnimalsApoptosisAutophagyBupivacaineCell Line, TumorCell ProliferationColorectal NeoplasmsHumansMaleMiceMice, NudeNF-kappa BSignal TransductionBupivacaineNF-kappa BapoptosisautophagyBupivacainecolorectal cancernf-κB

Identifiers

PMID34151717
PMCPMC8806862
OpenAlexW3174871445

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.