Evidence map›Paper›PMID 33490663›Full record

ArticleHeliyon2021

Progranulin depletion inhibits proliferation via the transforming growth factor beta/SMAD family member 2 signaling axis in Kasumi-1 cells.

Kuniaki Yabe, Yasuko Yamamoto, Masao Takemura, Takeshi Hara, Hisashi Tsurumi, Ginette Serrero, Toshitaka Nabeshima, Kuniaki Saito

Abstract read
In one paragraph

Article in Heliyon, 2021. 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
–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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Journal of microbiology and biotechnology · 2022
    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

8 authors.

Kuniaki YabeDepartment of Disease Control and Prevention, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.
Yasuko YamamotoDepartment of Disease Control and Prevention, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.
Masao TakemuraAdvanced Diagnostic System Research Laboratory, Fujita Health University, Graduate School of Health Sciences, Aichi, Japan.
Takeshi HaraDepartment of Hematology, Matsunami General Hospital, Gifu, Japan.
Hisashi TsurumiDepartment of Hematology, Matsunami General Hospital, Gifu, Japan.
Ginette SerreroUniversity of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD, USA.
Toshitaka NabeshimaAdvanced Diagnostic System Research Laboratory, Fujita Health University, Graduate School of Health Sciences, Aichi, Japan.
Kuniaki SaitoDepartment of Disease Control and Prevention, Fujita Health University Graduate School of Health Sciences, Aichi, Japan.

Funding

Pharmacology & human Phase 1 safety & dose escalation studies using anti-GP88 in aggressive breast cancerR44CA224718 · NCI · A AND G PHARMACEUTICAL, INC. · PI SERRERO, GINETTE · 2018 to 2022
$2.0M
Targeted Therapy for Non Small Cell Lung Carcinoma: Human Phase 1 safety and dose escalation studiesR44CA162629 · NCI · A AND G PHARMACEUTICAL, INC. · PI SERRERO, GINETTE · 2017 to 2018
$2.0M
NCI NIH HHS R44 CA162629NCI NIH HHS R44 CA224718
6 · The paper itself

Abstract

Progranulin is an autocrine growth factor that promotes proliferation, migration, invasion, and chemoresistance of various cancer cells. These mechanisms mainly depend on the protein kinase B (Akt)/mechanistic target of rapamycin (mTOR) pathway. Recent studies have shown that patients with hematopoietic cancer have elevated serum progranulin levels. Thus, the current study aimed to investigate the role of progranulin in hematopoietic cancer cells and how it modulates their proliferation. Both knockdown of progranulin and progranulin neutralizing antibody treatment inhibited proliferation in several human hematopoietic cancer cell lines. Moreover, progranulin depletion not only decreases the phosphorylation level of the Akt/mTOR pathway but also, surprisingly, increases the expression of transforming growth factor-beta (TGF-β) and phosphorylation of mothers against decapentaplegic homolog 2 (SMAD2) in Kasumi-1 cell. Furthermore, LY2109761, an inhibitor of TGF-β receptor type I/II kinase, and TGF-β neutralizing antibody blocked the inhibition of proliferation induced by progranulin depletion. These data provide new insights that progranulin alters cell proliferation via the TGF-β axis and progranulin could be a new therapeutic target for hematopoietic cancers.

Indexed as

Hematologic neoplasmsMechanistic target of rapamycin complex 1ProgranulinTransforming growth factor beta

Identifiers

PMID33490663
PMCPMC7809376

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Registered trials

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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.