Evidence map›Paper›PMID 31547522›Full record

ArticleMolecules (Basel, Switzerland)2019

Ursolic and Oleanolic Acids Induce Mitophagy in A549 Human Lung Cancer Cells.

Nayeli Shantal Castrejón-Jiménez, Kahiry Leyva-Paredes, Shantal Lizbeth Baltierra-Uribe, Juan Castillo-Cruz, Marcia Campillo-Navarro, Alma Delia Hernández-Pérez, Alexandra Berenice Luna-Angulo, Rommel Chacón-Salinas, Ramón Mauricio Coral-Vázquez, Iris Estrada-García and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 73 citations in OpenAlex.

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  18. Aging · 2023
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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

13 authors at 4 institutions in 1 country.

Nayeli Shantal Castrejón-JiménezDepartamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. naye_nice85@hotmail.com.
Kahiry Leyva-ParedesDepartamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. kahiryley@hotmail.com.
Shantal Lizbeth Baltierra-UribeDepartamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. shantal_baliz@hotmail.com.ORCID 0000-0001-7490-0042
Juan Castillo-CruzDepartamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. juancast0508@gmail.com.
Marcia Campillo-NavarroDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. marcy265@hotmail.com.
Alma Delia Hernández-PérezDepartamento de Anatomía Patológica, Instituto Nacional de Rehabilitación, México-Xochimilco No. 289. Arenal de Guadalupe, Ciudad de México 14389, Mexico. almadeliahp@gmail.com.ORCID 0000-0003-4913-7203
Alexandra Berenice Luna-AnguloDepartamento de Neurociencias, Instituto Nacional de Rehabilitación, México-Xochimilco No. 289, Arenal de Guadalupe, Ciudad de México 14389, Mexico. lunangulo@gmail.com.
Rommel Chacón-SalinasDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. rommelchacons@yahoo.com.mx.ORCID 0000-0002-4500-0253
Ramón Mauricio Coral-VázquezSección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional, Salvador Díaz Mirón esq. Plan de San Luis S/N, Miguel Hidalgo, Casco de Santo Tomas, Ciudad de México 11340, Mexico. rmcoralv@gmail.com.
Iris Estrada-GarcíaDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. iestrada5@hotmail.com.
Luvia Enid Sánchez-TorresDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. luviasanchez@hotmail.com.ORCID 0000-0002-7128-849X
Carlos Torres-TorresSección de Estudios de Posgrado e Investigación, Escuela Superior de Ingeniería Mecánica y Eléctrica Unidad Zacatenco, Instituto Politécnico Nacional, Gustavo A. Madero, Ciudad de México 07738, Mexico. ctorrest@ipn.mx.ORCID 0000-0001-9255-2416
Blanca Estela García-PérezDepartamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Ciudad de México 11340, Mexico. abrilestela@hotmail.com.
Instituto Politécnico Nacional · MXInstituto Nacional de Rehabilitación · MXInstituto Nacional de Enfermedades Respiratorias · MXUniversidad Autónoma del Estado de Hidalgo · MX

Funding

Consejo Nacional de Ciencia y Tecnología 222001Secretaría de Investigación y Posgrado, Instituto Politécnico Nacional 20196609
6 · The paper itself

Abstract

Ursolic and oleanolic acids are natural isomeric triterpenes known for their anticancer activity. Here, we investigated the effect of triterpenes on the viability of A549 human lung cancer cells and the role of autophagy in their activity. The induction of autophagy, the mitochondrial changes and signaling pathway stimulated by triterpenes were systematically explored by confocal microscopy and western blotting. Ursolic and oleanolic acids induce autophagy in A549 cells. Ursolic acid activates AKT/mTOR pathways and oleanolic acid triggers a pathway independent on AKT. Both acids promote many mitochondrial changes, suggesting that mitochondria are targets of autophagy in a process known as mitophagy. The PINK1/Parkin axis is a pathway usually associated with mitophagy, however, the mitophagy induced by ursolic or oleanolic acid is just dependent on PINK1. Moreover, both acids induce an ROS production. The blockage of autophagy with wortmannin is responsible for a decrease of mitochondrial membrane potential (Δψ) and cell death. The wortmannin treatment causes an over-increase of p62 and Nrf2 proteins promote a detoxifying effect to rescue cells from the death conducted by ROS. In conclusion, the mitophagy and p62 protein play an important function as a survival mechanism in A549 cells and could be target to therapeutic control.

Indexed as

A549 CellsHumansMitophagyOleanolic AcidProtein KinasesPTEN-Induced Putative KinaseReactive Oxygen SpeciesTriterpenesUbiquitin-Protein LigasesUrsolic AcidOleanolic Acidparkin proteinProtein KinasesPTEN-Induced Putative KinaseReactive Oxygen SpeciesTriterpenesUbiquitin-Protein LigasesUrsolic AcidA549 human lung cancer cellsmitophagyoleanolic acidPINK1/Parkinreactive oxygen speciesursolic acid

Identifiers

PMID31547522
PMCPMC6803966
OpenAlexW2973346642

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.