Evidence map›Paper›PMID 35794842›Full record

ArticleCell proliferation2022

Inhibition of L-type voltage-gated calcium channel-mediated Ca

Shujin Li, Hyun-Yi Kim, Dong-Joon Lee, Sung-Ho Park, Keishi Otsu, Hidemitsu Harada, Young-Soo Jung, Han-Sung Jung

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Calcium channels as pharmacological targets for cancer therapy.Clinical and experimental medicine · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. 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

8 authors at 3 institutions in 2 countries.

Shujin LiDivision in Anatomy and Developmental Biology, Department of Oral Biology, Taste Research Center, Oral Science Research Center, BK21 FOUR Project, Yonsei University College of Dentistry, Seoul, South Korea.ORCID https://orcid.org/0000-0002-8818-5411
Hyun-Yi KimNGeneS Inc, Ansan-si, Gyeonggi-do, South Korea.
Dong-Joon LeeDivision in Anatomy and Developmental Biology, Department of Oral Biology, Taste Research Center, Oral Science Research Center, BK21 FOUR Project, Yonsei University College of Dentistry, Seoul, South Korea.ORCID https://orcid.org/0000-0001-6532-9729
Sung-Ho ParkDepartment of Oral & Maxillofacial Surgery, Yonsei University College of Dentistry, Seoul, South Korea.
Keishi OtsuDivision of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, Iwate, Japan.
Hidemitsu HaradaDivision of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, Iwate, Japan.
Young-Soo JungDepartment of Oral & Maxillofacial Surgery, Yonsei University College of Dentistry, Seoul, South Korea.
Han-Sung JungDivision in Anatomy and Developmental Biology, Department of Oral Biology, Taste Research Center, Oral Science Research Center, BK21 FOUR Project, Yonsei University College of Dentistry, Seoul, South Korea.ORCID https://orcid.org/0000-0003-2795-531X
Yonsei University · KRIwate Medical University · JPAnsan University · KR

Funding

National Research Foundation of Korea NRF-2016R1A5A2008630National Research Foundation of Korea NRF-2022R1A2B5B03001627
6 · The paper itself

Abstract

objectivesAmeloblastoma (AM) has been known as a benign but locally invasive tumour with high recurrence rates. Invasive behaviour of the AM results in destruction of the adjacent jawbone and the non-detectable remnants during surgery, interrupting the complete elimination of cancer cells.

methodsTo explore novel targets for the tumour cell invasion, a transcriptomic analysis between AM and odontogenic keratocyst were performed through next-generation sequencing in detail.

resultsEnrichment of CACNA1C gene (encoding Cav1.2) in AM, a subunit of the L-type voltage-gated calcium channel (VGCC) was observed for the first time. The expression and channel activity of Cav1.2 was confirmed by immunostaining and calcium imaging in the patient samples or primary cells. Verapamil, L-type VGCC blocker revealed suppression of the Ca

conclusionTaken together, Cav1.2 maybe considered to be a therapeutic candidate to decrease the collective migration and invasion of AM.

Indexed as

AmeloblastomaCalcium Channel BlockersCalcium Channels, L-TypeAnimalsCalciumCalcium SignalingHumansVerapamilCACNA1C protein, humanCalciumCalcium Channel BlockersCalcium Channels, L-TypeVerapamil

Identifiers

PMID35794842
PMCPMC9628225
OpenAlexW4284886955

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.