Evidence map›Paper›PMID 28031534›Full record

ArticleOncotarget2017

Autophagy inhibition enhances photocytotoxicity of Photosan-II in human colorectal cancer cells.

Li Xiong, Zhipeng Liu, Guoqing Ouyang, Liangwu Lin, He Huang, Hongxiang Kang, Wei Chen, Xiongying Miao, Yu Wen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

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  19. The Roles of Autophagy in Cancer.International journal of molecular sciences · 2018
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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

9 authors at 4 institutions in 2 countries.

Li XiongGeneral Surgery Department of Second Xiangya Hospital, Central South University, Changsha, HN, China.
Zhipeng LiuGeneral Surgery Department of Second Xiangya Hospital, Central South University, Changsha, HN, China.
Guoqing OuyangGeneral Surgery Department of Second Xiangya Hospital, Central South University, Changsha, HN, China.
Liangwu LinChina State Key Laboratory for Powder Metallurgy, Central South University, Changsha, HN, China.
He HuangDepartment of Histology and Embryology, Xiangya School of Medicine, Central South University, Changsha, HN, China.
Hongxiang KangInstitute of Radiation Medicine, Academy of Military Medical Sciences, Beijing, China.
Wei ChenDepartment of Physics, University of Texas at Arlington, Arlington, TX, USA.
Xiongying MiaoGeneral Surgery Department of Second Xiangya Hospital, Central South University, Changsha, HN, China.
Yu WenGeneral Surgery Department of Second Xiangya Hospital, Central South University, Changsha, HN, China.
Central South University · CNSecond Xiangya Hospital of Central South University · CNAcademy of Military Medical Sciences · CNThe University of Texas at Arlington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photodynamic therapy (PDT) has emerged as an attractive therapeutic treatment for colorectal cancer because of its accessibility through endoscopy and its ability to selectively target tumors without destroying the anatomical integrity of the colon. We therefore investigated the therapeutic relevance of the interplay between autophagy and apoptosis in Photosan-II (PS-II)-mediated photodynamic therapy (PS-PDT) in in vitro and in vivo models for human colorectal cancer. We observed that PS-PDT-induced dose-dependently triggered apoptosis and autophagy in both SW620 and HCT116 cells. PS-PDT-treated SW620 cells exhibited nuclear condensation and increased levels of cleaved caspase-3, PARP and Bax, which is reminiscent of apoptosis. PS-PDT also induced autophagic vacuoles, double membrane autophagosome structures and the autophagy-related proteins P62, Bcl-2, ATG7 and LC3-II. In addition, the AKT-mTOR pathway was downregulated, while AMPK was upregulated in PS-PDT-treated cells. Inhibiting autophagy using chloroquine or by downregulating ATG7 using shRNA further upregulated apoptosis, suggesting autophagy was probably was protective to PS-PDT-treated tumor cells. In vivo relevance was demonstrated when a combination of chloroquine and PS-PDT significantly reduced the tumor size in a xenograft mice model. Our findings demonstrate that combination therapy using PS-PDT and autophagy inhibitors may be an effective approach to treating colorectal cancer patients.

Indexed as

PhotochemotherapyAnimalsAntineoplastic Combined Chemotherapy ProtocolsApoptosisApoptosis Regulatory ProteinsAutophagyAutophagy-Related ProteinsCell ProliferationChloroquineColorectal NeoplasmsDose-Response Relationship, DrugFemaleGene Expression Regulation, NeoplasticHCT116 CellsHumansInhibitory Concentration 50Apoptosis Regulatory ProteinsAutophagy-Related ProteinsChloroquinePhotosensitizing Agentsapoptosisautophagycolorectal cancerphotodynamic therapyPhotosan-II

Identifiers

PMID28031534
PMCPMC5351642
OpenAlexW2561259127

What OpenQuestion holds

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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.