Evidence map›Paper›PMID 27260851›Full record

ArticleCancer biology & therapy2016

Dehydroepiandrosterone inhibits events related with the metastatic process in breast tumor cell lines.

Rebeca López-Marure, Estrella Zapata-Gómez, Leticia Rocha-Zavaleta, María Cecilia Aguilar, Magali Espinosa Castilla, Jorge Meléndez Zajgla, Noemí Meraz-Cruz, Claudia Huesca-Gómez, Ricardo Gamboa-Ávila, Erika Olivia Gómez-González

Abstract read
In one paragraph

Article in Cancer biology & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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.

Rebeca López-Marurea Departamento de Fisiología , Instituto Nacional de Cardiología "Ignacio Chávez," Ciudad de México , México.
Estrella Zapata-Gómeza Departamento de Fisiología , Instituto Nacional de Cardiología "Ignacio Chávez," Ciudad de México , México.
Leticia Rocha-Zavaletab Departamento de Biología Molecular y Biotecnología , Instituto de Investigaciones Biomédicas , UNAM , Ciudad de México , México.
María Cecilia Aguilarb Departamento de Biología Molecular y Biotecnología , Instituto de Investigaciones Biomédicas , UNAM , Ciudad de México , México.
Magali Espinosa Castillac Laboratorio de Genómica Funcional del Cáncer , Instituto Nacional de Medicina Genómica , Ciudad de México , México.
Jorge Meléndez Zajglac Laboratorio de Genómica Funcional del Cáncer , Instituto Nacional de Medicina Genómica , Ciudad de México , México.
Noemí Meraz-Cruzd Unidad de Vinculación Científica , Facultad de Medicina , UNAM , Ciudad de Mexico , México.
Claudia Huesca-Gómeza Departamento de Fisiología , Instituto Nacional de Cardiología "Ignacio Chávez," Ciudad de México , México.
Ricardo Gamboa-Ávilaa Departamento de Fisiología , Instituto Nacional de Cardiología "Ignacio Chávez," Ciudad de México , México.
Erika Olivia Gómez-Gonzáleze Academia de Biología , Colegio de Ciencias y Humanidades, Universidad Autónoma de la Ciudad de México , Ciudad de México , México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dehydroepiandrosterone (DHEA), an adrenal hormone, has a protective role against cancer. We previously shown that DHEA inhibits the proliferation and migration of cell lines derived from breast cancer; however, the role of DHEA in others events related with these effects are unknown. We hypothesized that DHEA inhibits the expression of proteins and some events related with cell migration and metastasis. We determined the migration in Boyden chambers, the invasion in matrigel, anchorage-independent growth and the formation of spheroids in 3 cell lines (MCF-7, MDA-MB-231, ZR-75-30) derived from breast cancer exposed to DHEA. The secretion of metalloproteinases (MMPs), tissue inhibitors of metalloproteinases (TIMPs), and several pro-inflammatory molecules in the secretome of these cells was also evaluated.  DHEA inhibited the migration in transwells and the invasion in matrigel of MCF-7 and MDA-MB-231 cells. Besides, DHEA inhibited the anchorage-independent growth on agar and decreased the size of spheroids, and also reduced the secretion of IL-1α, IL-6, IL-8, and TNF-α in all cell lines. Metalloproteinase-1 (MMP-1) secretion was slightly decreased by DHEA treatment in MDA-MB-231 cells. Our results also showed that inhibition of migration and invasion induced by DHEA in breast cancer cells is correlated with the decrease of cytokine/chemokine secretion and the diminution of tumor cells growth.  MCF-7 cells were the most responsive to the exposure to DHEA, whereas ZR-75-30 cells responded less to this hormone, suggesting that DHEA could be used in the treatment of breast cancer in early stages.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCell Growth ProcessesCell Line, TumorCell MovementDehydroepiandrosteroneFemaleHumansMCF-7 CellsNeoplasm MetastasisDehydroepiandrosteroneBreast cancerDehydroepiandrosteroneinvasionmetastasismigration

Identifiers

PMID27260851
PMCPMC5036408

What OpenQuestion holds

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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.