Evidence map›Paper›PMID 33767160›Full record

ArticleCell death & disease2021

Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids.

Martina Lepore Signorile, Valentina Grossi, Simone Di Franco, Giovanna Forte, Vittoria Disciglio, Candida Fasano, Paola Sanese, Katia De Marco, Francesco Claudio Susca, Laura Rosa Mangiapane and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Understanding and overcoming multidrug resistance in cancer.Nature reviews. Clinical oncology · 2025
    Review
  6. Review
  7. Article
  8. Role of CELF2 in ferroptosis: Potential targets for cancer therapy (Review).International journal of molecular medicine · 2023
    Review
  9. Dysregulated Signalling Pathways Driving Anticancer Drug Resistance.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Atypical p38 Signaling, Activation, and Implications for Disease.International journal of molecular sciences · 2021
    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

18 authors at 4 institutions in 1 country.

Martina Lepore Signorile *Medical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Valentina Grossi *Medical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy. grossi.labsimone@gmail.com.
Simone Di FrancoCellular & Molecular Pathophysiology Laboratory, Department of Surgical & Oncological Sciences, University of Palermo, 90127, Palermo, Italy.
Giovanna ForteMedical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Vittoria DisciglioMedical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Candida FasanoMedical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Paola SaneseMedical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Katia De MarcoMedical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Francesco Claudio SuscaMedical Genetics, Department of Biomedical Sciences and Human Oncology (DIMO), University of Bari Aldo Moro, 70124, Bari, Italy.
Laura Rosa MangiapaneCellular & Molecular Pathophysiology Laboratory, Department of Surgical & Oncological Sciences, University of Palermo, 90127, Palermo, Italy.
Annalisa NicotraCellular & Molecular Pathophysiology Laboratory, Department of Surgical & Oncological Sciences, University of Palermo, 90127, Palermo, Italy.
Gabriella Di CarloDepartment of Emergency and Organ Transplantation, Operating Unit of Pathological Anatomy, University of Bari Aldo Moro, 70124, Bari, Italy.
Francesco DituriPersonalized Medicine, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Gianluigi GiannelliPersonalized Medicine, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy.
Giuseppe IngravalloDepartment of Emergency and Organ Transplantation, Operating Unit of Pathological Anatomy, University of Bari Aldo Moro, 70124, Bari, Italy.
Gianluca CanettieriDepartment of Molecular Medicine, Sapienza University of Rome, 00161, Rome, Italy.
Giorgio StassiCellular & Molecular Pathophysiology Laboratory, Department of Surgical & Oncological Sciences, University of Palermo, 90127, Palermo, Italy.
Cristiano SimoneMedical Genetics, National Institute for Gastroenterology, IRCCS 'S. de Bellis' Research Hospital, 70013, Castellana Grotte (Ba), Italy. cristianosimone73@gmail.com.ORCID http://orcid.org/0000-0002-2628-7658
Gastroenterology Hospital "Saverio de Bellis" · ITUniversity of Palermo · ITUniversity of Bari Aldo Moro · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of locally advanced colorectal cancer (CRC) is currently unsatisfactory. This is mainly due to drug resistance, recurrence, and subsequent metastatic dissemination, which are sustained by the cancer stem cell (CSC) population. The main driver of the CSC gene expression program is Wnt signaling, and previous reports indicate that Wnt3a can activate p38 MAPK. Besides, p38 was shown to feed into the canonical Wnt/β-catenin pathway. Here we show that patient-derived locally advanced CRC stem cells (CRC-SCs) are characterized by increased expression of p38α and are "addicted" to its kinase activity. Of note, we found that stage III CRC patients with high p38α levels display reduced disease-free and progression-free survival. Extensive molecular analysis in patient-derived CRC-SC tumorspheres and APC

Indexed as

beta CateninChromatinColorectal NeoplasmsHumansMitogen-Activated Protein Kinase 14Neoplastic Stem CellsOrganoidsPrognosisProtein Processing, Post-Translationalbeta CateninChromatinMitogen-Activated Protein Kinase 14

Identifiers

PMID33767160
PMCPMC7994846
OpenAlexW3138816287

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.