Evidence map›Paper›PMID 33215275›Full record

ArticleMedical oncology (Northwood, London, England)2020

Proteasome inhibitors attenuates mitoxantrone-triggered immunogenic cell death in prostate cancer cells.

Wei Wei, Haibin Li, Guoan Zhang, Ying Zhang, Ke Wu, Rongrong Bao, Gege Wang, Han Zheng, Yong Xia, Changlin Li

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Anti-tumor effect of proteasome inhibitor on canine urothelial carcinoma.The Journal of veterinary medical science · 2024
    Article
  5. Review
  6. 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 at 1 institution in 1 country.

Wei WeiCenter for Experimental Medicine, School of Public Health, Jining Medical University, Jining, 272067, China.
Haibin LiInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Guoan ZhangInstitute of Cancer Pathology Research, Jining Medical University, Jining, 272067, China.
Ying ZhangInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Ke WuInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Rongrong BaoInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Gege WangInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Han ZhengInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Yong XiaInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China.
Changlin LiInstitute of Precision Medicine, Jining Medical University, Jining, 272067, China. changlinli@mail.jnmc.edu.cn.ORCID http://orcid.org/0000-0001-5872-6443
Jining Medical University · CN

Funding

Natural Science Foundation of Shandong Province ZR2016CB49Natural Science Foundation of Shandong Province ZR2016CQ01Natural Science Foundation of Shandong Province ZR2016HL25
6 · The paper itself

Abstract

Both mitoxantrone (MTX) and proteasome inhibitors efficiently trigger immunogenic cell death (ICD) in cancer cells. However, whether the combination of MTX and proteasome inhibitors can synergistically enhance ICD remains unknown. In this study, we showed that the proteasome inhibitors bortezomib (BZM) and carbobenzoxy-L-leucyl-L-leucyl-L-leucinal (MG132) impaired MTX-induced ICD in prostate cancer cells, as measured using ICD biomarkers and dendritic cell activation in vitro. Mice vaccinated with RM-1 mouse prostate cancer cell line treated with BZM or MG132 in combination with MTX showed enhanced tumor growth, and shortened tumor-free, and worse overall survival compared with those treated with MTX alone. In conclusion, we demonstrated that proteasome inhibitors (BZM or MG132) attenuated MTX-induced ICD, suggesting that proteasome activation was required for MTX-induced ICD.

Indexed as

AnimalsBortezomibCell Line, TumorHumansImmunogenic Cell DeathMaleMiceMice, Inbred C57BLMitoxantronePhagocytosisProstatic NeoplasmsProteasome InhibitorsBortezomibMitoxantroneProteasome InhibitorsBortezomibImmunogenic cell deathMitoxantroneProteasome inhibitor

Identifiers

PMID33215275
OpenAlexW3098253716

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.