Evidence map›Paper›PMID 36632591›Full record

ReviewCancer diagnosis & prognosis

Involvement of the PRL-PAK1 Pathway in Cancer Cell Migration.

Jessica Mariana Carrasco-Ceballos, David Barrera-Hernández, José Locia-Espinosa, Clara Luz Sampieri, Jesús Antonio Lara-Reyes, María Elena Hernández-Aguilar, Gonzalo Emiliano Aranda-Abreu, María Rebeca Toledo-Cárdenas, Lizbeth Donají Chi-Castañeda, Cesar Antonio Pérez-Estudillo and 1 more

Open access · greenAbstract readReview
In one paragraph

Review in Cancer diagnosis & prognosis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

11 authors at 1 institution in 1 country.

Jessica Mariana Carrasco-CeballosDoctorado en Investigaciones Cerebrales, Instituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
David Barrera-HernándezDepartamento de Biología de la Reproducción "Dr. Carlos Gual Castro", Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, México.
José Locia-EspinosaFacultad de Química Farmacéutica Biológica, Universidad Veracruzana, Xalapa, México.
Clara Luz SampieriInstituto de Salud Pública, Universidad Veracruzana, Xalapa, México.
Jesús Antonio Lara-ReyesInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
María Elena Hernández-AguilarInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
Gonzalo Emiliano Aranda-AbreuInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
María Rebeca Toledo-CárdenasInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
Lizbeth Donají Chi-CastañedaInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
Cesar Antonio Pérez-EstudilloInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
Fausto Rojas-DuránInstituto de Investigaciones Cerebrales, Universidad Veracruzana, Xalapa, México.
Universidad Veracruzana · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prolactin (PRL) is a polypeptide hormone synthesized in the lactotrophs of the adenohypophysis and in extrahypophyseal glands (such as the prostate and breasts) where it promotes their development. PRL is also involved in cancer development in these glands. It has been shown to stimulate cancer cell migration, suggesting its possible involvement in metastasis, in which cell migration plays an essential role. However, the role of PRL in cell migration is still unclear. Moreover, the intracellular mechanisms activated by PRL to carry out cell migration are less well understood. PRL exerts its effects via the PRL receptor (PRLR), which leads intracellularly to phosphorylation of Janus protein kinase 2 (JAK2), which in turn phosphorylates p21-activated protein kinase (PAK1), leading to an increase in cell migration. Although several studies have described the involvement of the PRL-PAK1 pathway in breast cancer cell migration, the molecular mechanisms have not been fully elucidated and there is no integration of these into signaling pathways. This study was conducted based on literature search of review articles and original research in the PubMed database, using the following keywords: PRL, cell migration, PRL and cell migration, PAK1 and signaling pathways. The aim of this review article was to describe the major signaling pathways controlled by PRL-PAK1 and propose a comprehensive model of the signaling pathways associated with PRL-PAK1.

Indexed as

cell migrationPAK1Prolactinreviewsignaling pathway

Identifiers

PMID36632591
PMCPMC9801455
OpenAlexW4313362989

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.