Evidence map›Paper›PMID 31766723›Full record

ArticleCancers2019

The Potential Impact of Connexin 43 Expression on Bcl-2 Protein Level and Taxane Sensitivity in Head and Neck Cancers-In Vitro Studies.

Bianka Gurbi, Diána Brauswetter, Attila Varga, Pál Gyulavári, Kinga Pénzes, József Murányi, Veronika Zámbó, Ede Birtalan, Tibor Krenács, David Laurence Becker and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. 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
0.3field-weighted citation impact, top 43% 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, 9 citations in OpenAlex.

  1. Review
  2. MEK Is a Potential Indirect Target in Subtypes of Head and Neck Cancers.International journal of molecular sciences · 2023
    Article
  3. Article
  4. Article
  5. 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 3 institutions in 2 countries.

Bianka GurbiDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0002-5635-6255
Diána BrauswetterDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0003-4199-282X
Attila VargaDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.
Pál GyulaváriDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.
Kinga PénzesDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.
József MurányiDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0001-5672-6482
Veronika ZámbóDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.
Ede BirtalanDepartment of Oto-Rhino-Laryngology, Head and Neck Surgery, Semmelweis University, H-1083 Budapest, Hungary.
Tibor KrenácsDepartment of Pathology and Experimental Cancer Research, Semmelweis University, H-1085 Budapest, Hungary.
David Laurence BeckerLee Kong Chian School of Medicine, Nanyang Technological University, Singapore 308232, Singapore.
Miklós CsalaDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0002-3829-4361
István Vályi-NagyCentral Hospital of Southern Pest National Institute of Hematology and Infectious Diseases, H-1097 Budapest, Hungary.
István PetákMTA-SE Pathobiochemistry Research Group, Semmelweis University, H-1094 Budapest, Hungary.
Kornél DánosDepartment of Oto-Rhino-Laryngology, Head and Neck Surgery, Semmelweis University, H-1083 Budapest, Hungary.
Semmelweis University · HUNanyang Technological University · SGNational Center for Epidemiology · HU

Funding

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal K-124813Nemzeti Kutatási Fejlesztési és Innovációs Hivatal K-128785Nemzeti Kutatási Fejlesztési és Innovációs Hivatal NVKP_16-1-2016-0005
6 · The paper itself

Abstract

The poor prognosis of head and neck squamous cell carcinoma (HNSCC) is partly due to the lack of reliable predictive markers. Connexin 43 (Cx43) protein and its cell-communication channels have been assigned tumor suppressor functions while the anti-apoptotic Bcl-2 (B-cell lymphoma-2) protein has been associated with negative prognostic significance in cancer. This study aimed to test the role of Cx43 protein on Bcl-2 expression, tumor progression and response to taxane-based treatment in HNSCC. Human papillomavirus (HPV) negative HNSCC cell lines were tested for paclitaxel sensitivity through measuring apoptosis induction, cell viability and changes in Cx43 and Bcl-2 levels using flow cytometry, cell viability assay, immunocytochemistry and western blot. Inhibition of Cx43 expression using siRNA increased Bcl-2 protein levels in SCC25 (tongue squamous cell carcinoma) cells, while forced Cx43 expression reduced Bcl-2 levels and supported paclitaxel cytotoxicity in FaDu (hypopharynx squamous cell carcinoma) cells. In vitro results were in line with protein expression and clinicopathological features tested in tissue microarray samples of HNSCC patients. Our data demonstrate that elevated Cx43 and reduced Bcl-2 levels may indicate HNSCC sensitivity to taxane-based treatments. On the contrary, silencing of the Cx43 gene

Indexed as

Bcl-2connexin 43head and neck cancerpaclitaxel

Identifiers

PMID31766723
PMCPMC6966683
OpenAlexW2991428559

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.