Evidence map›Paper›PMID 29869056›Full record

ArticleIn vitro cellular & developmental biology. Animal2018

L-carnosine induces apoptosis/cell cycle arrest via suppression of NF-κB/STAT1 pathway in HCT116 colorectal cancer cells.

Jooyeon Lee, Jeong-Ran Park, Hanbyeol Lee, Soojin Jang, Se-Min Ryu, Hyejin Kim, Donguk Kim, Aera Jang, Se-Ran Yang

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Erythrocytes Prevent Degradation of Carnosine by Human Serum Carnosinase.International journal of molecular sciences · 2021
    Article
  10. Review
  11. Article
  12. 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

9 authors at 1 institution in 1 country.

Jooyeon LeeDepartment of Thoracic and Cardiovascular Surgery, Kangwon National University, Chuncheon, 24341, South Korea.
Jeong-Ran ParkDepartment of Thoracic and Cardiovascular Surgery, Kangwon National University, Chuncheon, 24341, South Korea.
Hanbyeol LeeDepartment of Thoracic and Cardiovascular Surgery, Kangwon National University, Chuncheon, 24341, South Korea.
Soojin JangDepartment of Thoracic and Cardiovascular Surgery, Kangwon National University, Chuncheon, 24341, South Korea.
Se-Min RyuDepartment of Thoracic and Cardiovascular Surgery, Kangwon National University, Chuncheon, 24341, South Korea.
Hyejin KimDepartment of Animal Products and Food Science, Kangwon National University, Chuncheon, 24341, South Korea.
Donguk KimDepartment of Animal Products and Food Science, Kangwon National University, Chuncheon, 24341, South Korea.
Aera JangDepartment of Animal Products and Food Science, Kangwon National University, Chuncheon, 24341, South Korea. ajang@kangwon.ac.kr.
Se-Ran YangDepartment of Thoracic and Cardiovascular Surgery, Kangwon National University, Chuncheon, 24341, South Korea. seran@kangwon.ac.kr.
Kangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

L-carnosine, a dipeptide of the amino acids β-alanine and histidine, is found in various tissues, such as the central nervous system and skeletal muscles. Recently, L-carnosine has been reported to possess anti-tumor activity; however, the molecular mechanism underlying its activity in colorectal cancer is still unknown. Therefore, we investigated the effect of L-carnosine using a human colorectal cancer cell line, HCT116. Treatment with L-carnosine (0, 100, or 200 mM) for 24 h gradually reduced cellular proliferation according to immunochemistry and 7-aminoactinomycin D (7-AAD) analyses and induced G0/G1 phase arrest. In the RT-PCR analysis, L-carnosine decreased the mRNA levels of cell cycle-related genes in HCT116 cells. In the Western blot analysis, levels of the cyclin D1, BAX/Bcl-2, cleaved caspase-3, p21, and p53 proteins were significantly increased in cells treated with L-carnosine. We next determined whether STAT1/NF-κB pathway is involved in regulation of cell cycle arrest- and cell death-associated gene in HCT116. The L-carnosine treatment significantly inhibited the phosphorylation of STAT1 on Tyr701 and NF-κB p65 on Ser276 and Ser536, and then, we exogenously blocked the NF-κB phosphorylation using Bay 11-7082. Based on our findings, L-carnosine induces cell cycle arrest and apoptosis in human colorectal cancer cells by suppressing of NF-κB/STAT1 signaling.

Indexed as

ApoptosisCarnosineCell Cycle CheckpointsCell ProliferationColorectal NeoplasmsCyclin-Dependent Kinase Inhibitor p21G1 PhaseHCT116 CellsHumansModels, BiologicalNF-kappa BPhosphorylationResting Phase, Cell CycleSTAT1 Transcription FactorTumor Suppressor Protein p53CarnosineCyclin-Dependent Kinase Inhibitor p21NF-kappa BSTAT1 protein, humanSTAT1 Transcription FactorTumor Suppressor Protein p53ApoptosisCell cycle arrestColorectal cancerL-carnosineNF-κB p65STAT1

Identifiers

PMID29869056
OpenAlexW2805679623

What OpenQuestion holds

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Registered trials

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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.