Evidence map›Paper›PMID 34337035›Full record

ArticleBioMed research international2021

Antitumor Effect of Lenvatinib Combined with Alisertib in Hepatocellular Carcinoma by Targeting the DNA Damage Pathway.

Jianwen Hao, Qizhen Peng, Keruo Wang, Ge Yu, Yi Pan, Xiaoling Du, Na Hu, Xuening Zhang, Yu Qin, Huikai Li

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Repurposed Drugs in Gastric Cancer.Molecules (Basel, Switzerland) · 2022
    Review
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

10 authors at 5 institutions in 1 country.

Jianwen HaoDepartment of Radiology, Tianjin Chest Hospital, Tianjin 300350, China.ORCID https://orcid.org/0000-0001-5340-8235
Qizhen PengDepartment of Radiology, Tungwah Hospital of Sun Yat-Sen University, Dongguan, 523000 Guangdong, China.ORCID https://orcid.org/0000-0002-9334-2186
Keruo WangDepartment of Diagnostics, Tianjin Medical University, Tianjin 300070, China.
Ge YuDepartment of Hepatobiliary, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy of Tianjin, Tianjin Clinical Research Center for Cancer, Tianjin 300070, China.
Yi PanDepartment of Pathology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy of Tianjin, Tianjin Clinical Research Center for Cancer, Tianjin 300070, China.
Xiaoling DuDepartment of Diagnostics, Tianjin Medical University, Tianjin 300070, China.
Na HuDepartment of Diagnostics, Tianjin Medical University, Tianjin 300070, China.
Xuening ZhangDepartment of Radiology Second Hospital of Tianjin Medical University, Tianjin 300070, China.ORCID https://orcid.org/0000-0002-4621-5731
Yu QinDepartment of Diagnostics, Tianjin Medical University, Tianjin 300070, China.ORCID https://orcid.org/0000-0002-1829-7864
Huikai LiDepartment of Hepatobiliary, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy of Tianjin, Tianjin Clinical Research Center for Cancer, Tianjin 300070, China.ORCID https://orcid.org/0000-0003-4864-4991
Tianjin Medical University · CNTianjin Medical University Cancer Institute and Hospital · CNSecond Hospital of Tianjin Medical University · CNTianjin Chest Hospital · CNTung Wah Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

methodsImmunohistochemical staining, sequencing, and genetic analysis of liver cancer tissues were performed. The antitumor efficacy of single-agent or combination treatment was measured by cell counting kit-8 assay and colony formation assays. Their antiproliferative and apoptosis activity is evaluated by cell cycle analyses and wound healing assays. The DNA-related proteins were also measured by Western blotting and immunohistochemical staining. The HepG2 xenograft model was used to detect the effects of lenvatinib-alisertib on the antitumor activity.

resultsAURKA was found to be upregulated in HCC tissues (77.3%, 17/22). Combined alisertib and lenvatinib treatment significantly enhanced the inhibition of proliferation and migration in HepG2 and Hep3B cell lines compared to single-agent treatments (all

conclusionsOur findings provide evidence for the possible use of alisertib in combination with lenvatinib in the treatment of HCC for better therapeutic outcomes.

Indexed as

DNA DamageAnimalsAntineoplastic AgentsApoptosisAurora Kinase AAzepinesCarcinoma, HepatocellularCell DeathCell ProliferationFemaleLiver NeoplasmsMiceMice, Inbred BALB CMice, NudeModels, BiologicalNeoplasm MetastasisAntineoplastic AgentsAurora Kinase AAzepineslenvatinibMLN 8237Phenylurea CompoundsPyrimidinesQuinolines

Identifiers

PMID34337035
PMCPMC8324353
OpenAlexW3185467428

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.