Evidence map›Paper›PMID 29900694›Full record

ArticleAdvanced healthcare materials2018

Cross Talk Between Autophagy and Apoptosis Contributes to ZnO Nanoparticle-Induced Human Osteosarcoma Cell Death.

Guanping He, Yunlong Ma, Ye Zhu, Lei Yong, Xiao Liu, Peng Wang, Chen Liang, Chenlong Yang, Zhigang Zhao, Bao Hai and 4 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Analyzing Molecular Determinants of Nanodrugs' Cytotoxic Effects.International journal of molecular sciences · 2025
    Pooled it
  2. Anticancer Activity of Green Synthesized ZnO Nanoparticles fromNanomaterials (Basel, Switzerland) · 2026
    Article
  3. Article
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  10. Enhanced Sensitivity of A549 Cells to Doxorubicin with WSInternational journal of molecular sciences · 2024
    Article
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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

14 authors.

Guanping HeDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Yunlong MaThe Center for Pain Medicine, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Ye ZhuDepartment of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, Norman, OK, 73019, USA.
Lei YongDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Xiao LiuDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Peng WangDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Chen LiangDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Chenlong YangDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Zhigang ZhaoDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Bao HaiDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Xiaoyu PanDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Zhongjun LiuDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Xiaoguang LiuDepartment of Orthopedics, Peking University Third Hospital, No. 49, North Garden Street, Haidian District, Beijing, 100191, China.
Chuanbin MaoDepartment of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, Norman, OK, 73019, USA.ORCID 0000-0002-8142-3659

Funding

Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Michael S. Businelle · 2018 to 2026
$27.1M
Virus-based nanoparticles for detecting breast cancer biomarkersR01EB021339 · NIBIB · UNIVERSITY OF OKLAHOMA · PI CAO, BINRUI · 2016 to 2019
$1.4M
Selective tumor inhibition by tumor-homing angiogenesis-suppressing nanofibersR21CA200504 · NCI · UNIVERSITY OF OKLAHOMA · PI MAO, CHUANBIN · 2015 to 2016
$361k
Hiring Non-toxic Virus Nanoparticles to Count Cancer Biomarker MoleculesR21CA195607 · NCI · UNIVERSITY OF OKLAHOMA · PI MAO, CHUANBIN · 2015 to 2016
$359k
National Natural Science Foundation of China 51673168National Natural Science Foundation of China 81472041NCI NIH HHS P30 CA225520NCI NIH HHS R21 CA195607NCI NIH HHS R21 CA200504NIBIB NIH HHS R01 EB021339NIH HHS CA195607NIH HHS CA200504NIH HHS EB021339
6 · The paper itself

Abstract

Killing osteosarcoma cells by zinc oxide nanoparticles (NPs) and its underlying subcellular mechanism are never studied. Here, it is found that the NPs induce cross talk between apoptosis and autophagy, which leads to osteosarcoma cell death. Specifically, the NP uptake promotes autophagy by inducing accumulation of autophagosomes along with impairment of lysosomal functions. The autophagy further causes the uptaken NPs to release zinc ions by promoting their dissolution. These intracellular zinc ions, together with those that are originally released from the extracellular NPs and flowed into the cells, collectively target and damage mitochondria to produce reactive oxygen species (ROS). Then the ROS inhibit cell proliferation by arresting S phase and trigger apoptosis by extrinsic and intrinsic pathways, ultimately leading to cell death. More importantly, suppression of the early stage autophagy restores cell viability by abolishing apoptosis whereas blockade of the late stage autophagy inversely enhances apoptosis. In contrast, inhibition of apoptosis shows a limited ability to restore cell viability but obviously enhance autophagy. Notably, cell viability is strongly ameliorated by the combination of inhibitors for both the late stage autophagy and the apoptosis. These findings provide a mechanistic understanding of the NP-directed autophagy and apoptosis in osteosarcoma cells.

Indexed as

ApoptosisAutophagyBlotting, WesternCaspase 3Cell Line, TumorCell ProliferationCell SurvivalHumansMetal NanoparticlesMicroscopy, Electron, TransmissionMicroscopy, FluorescenceOsteosarcomaOxidative StressReactive Oxygen SpeciesZinc OxideCaspase 3Reactive Oxygen SpeciesZinc Oxideapoptosisautophagycross talkhuman osteosarcoma cellszinc oxide nanoparticles

Identifiers

PMID29900694
PMCPMC6310009

What OpenQuestion holds

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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.