Evidence map›Paper›PMID 34606419›Full record

ArticleCell cycle (Georgetown, Tex.)2021

Cdc25C/cdc2/cyclin B, raf/MEK/ERK and PERK/eIF2α/CHOP pathways are involved in forskolin-induced growth inhibition of MM.1S cells by G2/M arrest and mitochondrion-dependent apoptosis.

Ping Yang, Pei-Wen Jiang, Chen Li, Ming-Xiang Gao, Yi-Song Sun, Dan-Ying Zhang, Wen-Qian Du, Jing Zhao, Song-Ting Shi, Yan Li and 3 more

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Ping YangSchool of Basic Medicine.
Pei-Wen JiangSchool of Basic Medicine.ORCID 0000-0001-6554-4592
Chen LiSchool of Basic Medicine.
Ming-Xiang GaoCenter of Science and Research.
Yi-Song SunSchool of Bioscience and Technology.
Dan-Ying ZhangSchool of Pharmacy.
Wen-Qian DuSchool of Pharmacy.
Jing ZhaoSchool of Pharmacy.
Song-Ting ShiSchool of Laboratory Medicine, Chengdu Medical College, Chengdu, China.
Yan LiSchool of Basic Medicine.
Tai YangCenter of Science and Research.
Li ChengSchool of Basic Medicine.
Min-Hui LiSchool of Basic Medicine.ORCID 0000-0002-3983-004X
Chengdu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) remains an incurable hematological malignancy characterized by proliferation and accumulation of plasma cells in the bone marrow. Innovative and effective therapeutic approaches that are able to improve the outcome and the survival of MM sufferers, especially the identification of novel natural compounds and investigation of their anti-MM mechanisms, are needed. Here, we investigated the effects and the potential mechanisms against MM of forskolin, a diterpene derived from the medicinal plant

Indexed as

ApoptosisColforsinG2 Phase Cell Cycle CheckpointsCell Line, TumorCyclin B1Eukaryotic Initiation Factor-2HumansMitochondriaMitogen-Activated Protein Kinase KinasesColforsinCyclin B1Eukaryotic Initiation Factor-2Mitogen-Activated Protein Kinase KinasesapoptosisforskolinG2/M arrestMultiple myelomanatural compounds

Identifiers

PMID34606419
PMCPMC8794531
OpenAlexW3203377788

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.