Evidence map›Paper›PMID 27942213›Full record

ArticleInternational journal of nanomedicine

Upregulation of Akt/NF-κB-regulated inflammation and Akt/Bad-related apoptosis signaling pathway involved in hepatic carcinoma process: suppression by carnosic acid nanoparticle.

Bo Tang, Fang Tang, Zhenran Wang, Guangying Qi, Xingsi Liang, Bo Li, Shengguang Yuan, Jie Liu, Shuiping Yu, Songqing He

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Effects ofMolecules (Basel, Switzerland) · 2026
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  3. Antibacterial Activity of Rosmarinic Acid AgainstAnimals : an open access journal from MDPI · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. lncRNA ENSRNOT00000087717 mediated differentiation of satellite glial cells derived from dorsal root ganglion via AKT1.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  12. Article
  13. Jingzhi Niuhuangjiedu Tablet Ameliorates Oral MucositisCombinatorial chemistry & high throughput screening · 2025
    Article
  14. Review
  15. Article
  16. Histochemistry for Molecular Imaging in Nanomedicine.International journal of molecular sciences · 2024
    Review
  17. Heliyon · 2024
    Article
  18. Article
  19. Liver cancer wars: plant-derived polyphenols strike back.Medical oncology (Northwood, London, England) · 2024
    Review
  20. Review

5 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Bo TangDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Fang TangDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Zhenran WangDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Guangying QiDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin, Guangxi, People's Republic of China.
Xingsi LiangDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Bo LiDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Shengguang YuanDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Jie LiuDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Shuiping YuDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Songqing HeDepartment of Hepatobiliary Surgery, Guilin Medical University Affiliated Hospital; Laboratory of Liver Injury and Repair Molecular Medicine, Guilin Medical University.
Guilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary liver cancer is globally the sixth most frequent cancer, and the second leading cause of cancer death and its incidence is increasing in many countries, becoming a serious threat to human health. Many researches focused on the treatment and prevention of liver cancer. However, due to the underlying molecular mechanism of liver cancer still not fully understood, the studies and development of treatments were forced to be delayed. Akt has been suggested to play an essential role in the progression of inflammation response and apoptosis. Hence, in this study, Akt-knockout mice and cells of liver cancer were used as a model to investigate the molecular mechanism of Akt-associated inflammatory and apoptotic signaling pathway linked with NF-κB and Bcl-2-associated death promoter (Bad) for the progression of liver cancer. Carnosic acid (CA), as a phenolic diterpene with anticancer, antibacterial, antidiabetic, as well as neuroprotective properties, is produced by many species from Lamiaceae family. Administration of CA nanoparticles was sufficient to lead to considerable inhibition of liver cancer progression. The results indicated that, compared to the normal liver cells, the expression of Akt was significantly higher in liver cancer cell lines. Also, we found that Akt-knockout cancer cell lines modulated inflammation response and apoptosis via inhibiting NF-κB activation and inducing apoptotic reaction. Our results indicated that the downstream signals, including cytokines regulated by NF-κB and caspase-3-activated apoptosis affected by Bad, were re-modulated for knockout of Akt. And CA nanoparticles, acting as Akt-knockout, could inhibit inflammation and accelerate apoptosis in liver cancer by altering NF-κB activation and activating caspase-3 through Bad pathway. These findings demonstrated that the nanoparticulate drug CA performed its effective role owing to its ability to reduce inflammatory action and enhance apoptosis for the overexpression of NF-κB and Bad via Akt signaling pathway, playing a direct role in liver cancer progression. Thus, nanoparticle CA might be an important and potential choice for the clinical treatment in the future.

Indexed as

AbietanesAnimalsAntioxidantsApoptosisbcl-Associated Death ProteinBlotting, WesternCarcinoma, HepatocellularCell AdhesionCell MovementCell ProliferationFemaleFlow CytometryFluorescent Antibody TechniqueHumansInflammationLiver NeoplasmsAbietanesAntioxidantsbcl-Associated Death ProteinNF-kappa BProto-Oncogene Proteins c-aktRNA, MessengersalvinAkt-knockoutapoptosiscarnosic acid nanoparticleinflammationliver cancer

Identifiers

PMID27942213
PMCPMC5138024
OpenAlexW2558925605

What OpenQuestion holds

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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.