Evidence map›Paper›PMID 30887517›Full record

ArticleInternational journal of cancer2019

Targeted therapy of the AKT kinase inhibits esophageal squamous cell carcinoma growth in vitro and in vivo.

Xuejiao Liu, Mengqiu Song, Penglei Wang, Ran Zhao, Hanyong Chen, Man Zhang, Yuanyuan Shi, Kangdong Liu, Fangfang Liu, Ran Yang and 4 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
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  8. Article
  9. Anticancer Potential of Natural Chalcones: In Vitro and In Vivo Evidence.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Article
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  13. Article
  14. Review
  15. Article
  16. Anticancer Activity of Natural and Synthetic Chalcones.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Review
  19. Review
  20. Article
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 at 4 institutions in 2 countries.

Xuejiao LiuSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Mengqiu SongSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Penglei WangSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Ran ZhaoSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Hanyong ChenThe Hormel Institute, University of Minnesota, Austin, Minnesota.
Man ZhangChina-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, China.
Yuanyuan ShiChina-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, China.
Kangdong LiuSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Fangfang LiuSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Ran YangChina-US (Henan) Hormel Cancer Institute, Zhengzhou, Henan, China.
Enmin LiDepartment of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou, Guangdong, China.
Ann M BodeThe Hormel Institute, University of Minnesota, Austin, Minnesota.
Zigang DongSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.
Mee-Hyun LeeSchool of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, China.ORCID 0000-0002-1216-0218
Zhengzhou University · CNUniversity of Minnesota · USChina-US (Henan) Hormel Cancer Institute · CNShantou University · CN

Funding

Chemoprevention of colon cancer by targeting the Wnt/beta-catenin pathwayR01CA187027 · NCI · UNIVERSITY OF MINNESOTA · PI KANG, NINGLING, ROH, EUNMIRI · 2015 to 2019
$1.7M
Prevention of solar UV-induced skin cancer by targeting LTA4HR01CA196639 · NCI · UNIVERSITY OF MINNESOTA · PI LIU, LIANG · 2015 to 2019
$1.7M
NCI NIH HHS R01 CA187027NCI NIH HHS R01 CA196639
6 · The paper itself

Abstract

Esophageal cancer, a leading cause of cancer death worldwide, is associated with abnormal activation of the AKT signaling pathway. Xanthohumol, a prenylated flavonoid tested in clinical trials, is reported to exert anti-diabetes, anti-inflammation and anticancer activities. However, the mechanisms underlying its chemopreventive or chemotherapeutic effects remain elusive. In the present study, we found that xanthohumol directly targeted AKT1/2 in esophageal squamous cell carcinoma (ESCC). Xanthohumol significantly inhibited the AKT kinase activity in an ATP competitive manner, which was confirmed in binding and computational docking models. KYSE70, 450 and 510 ESCC cell lines highly express AKT and knockdown of AKT1/2 suppressed proliferation of these cells. Treatment with xanthohumol inhibited ESCC cell growth and induced apoptosis and cell cycle arrest at the G1 phase. Xanthohumol also decreased expression of cyclin D1 and increased the levels of cleaved caspase-3, -7 and -PARP as well as Bax, Bim

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Cycle CheckpointsCell Line, TumorCell ProliferationCell SurvivalEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleFlavonoidsG1 PhaseHumansMiceMice, SCIDPropiophenonesAntineoplastic AgentsFlavonoidsPropiophenonesProto-Oncogene Proteins c-aktxanthohumolAKT signaling pathwayesophageal squamous cell carcinomatargeting AKT kinase activityxanthohumol

Identifiers

PMID30887517
PMCPMC6618024
OpenAlexW2923943493

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.