Evidence map›Paper›PMID 29969944›Full record

ArticleAutophagy2018

Rocaglamide enhances NK cell-mediated killing of non-small cell lung cancer cells by inhibiting autophagy.

Chao Yao, Zhongya Ni, Chenyuan Gong, Xiaowen Zhu, Lixin Wang, Zihang Xu, Chunxian Zhou, Suyun Li, Wuxiong Zhou, Chunpu Zou and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 77 citations in OpenAlex.

  1. Umbilical cord blood-derived natural killer cells:Annals of medicine and surgery (2012) · 2026
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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

11 authors at 1 institution in 1 country.

Chao Yaoa Laboratory of Integrative Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Zhongya Nia Laboratory of Integrative Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Chenyuan Gonga Laboratory of Integrative Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Xiaowen Zhua Laboratory of Integrative Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Lixin Wangb Department of Immunology and Pathogenic Biology , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Zihang Xuc Department of Internal Classic of Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Chunxian Zhoud Department of Pathology , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Suyun Lid Department of Pathology , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Wuxiong Zhoue Department of Histology and Embryology , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Chunpu Zouc Department of Internal Classic of Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Shiguo Zhua Laboratory of Integrative Medicine , School of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine , Shanghai , P. R. China.
Shanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting macroautophagy/autophagy is a novel strategy in cancer immunotherapy. In the present study, we showed that the natural product rocaglamide (RocA) enhanced natural killer (NK) cell-mediated lysis of non-small cell lung cancer (NSCLC) cells in vitro and tumor regression in vivo. Moreover, this effect was not related to the NK cell recognition of target cells or expressions of death receptors. Instead, RocA inhibited autophagy and restored the level of NK cell-derived GZMB (granzyme B) in NSCLC cells, therefore increasing their susceptibility to NK cell-mediated killing. In addition, we further identified that the target of RocA was ULK1 (unc-51 like autophagy activating kinase 1) that is required for autophagy initiation. Using firefly luciferase containing the 5´ untranslated region of ULK1, we found that RocA inhibited the protein translation of ULK1 in a sequence-specific manner. Taken together, RocA could block autophagic immune resistance to NK cell-mediated killing, and our data suggested that RocA was a promising therapeutic candidate in NK cell-based cancer immunotherapy.

Indexed as

AutophagyAnimalsAutophagy-Related Protein-1 HomologBenzofuransCarcinoma, Non-Small-Cell LungCell DegranulationGranzymesHumansKiller Cells, NaturalLung NeoplasmsMaleMice, Inbred C57BLMice, SCIDModels, BiologicalProtein BiosynthesisReceptors, Death DomainAutophagy-Related Protein-1 HomologBenzofuransGranzymesReceptors, Death DomainrocaglamideAutophagycancer immunotherapyimmune resistancenatural killer cellsnon-small cell lung cancerrocaglamide

Identifiers

PMID29969944
PMCPMC6135631
OpenAlexW2811096407

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.