Evidence map›Paper›PMID 32626964›Full record

ArticleMolecular medicine reports2020

Echinacoside promotes the proliferation of human renal tubular epithelial cells by blocking the HBX/TREM2‑mediated NF‑κB signalling pathway.

Yufan Zhang, Qinfang Wu, Limin Zhong, Lei Wang, Dongwei Gong

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. TREM2-driven peripheral macrophage regulation in inflammatory diseases: implications extending beyond neurological disorders.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  3. Review
  4. Review
  5. HBx-induced PLARenal failure · 2023
    Article
  6. Article
  7. Review
  8. The Role of HBx Protein in Diseases Beyond the Liver.Infection and drug resistance · 2023
    Review
  9. 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

5 authors at 1 institution in 1 country.

Yufan Zhang *Department of Traditional Chinese Medicine, Yangpu District Kongjiang Hospital, Shanghai 200093, P.R. China.
Qinfang Wu *Department of Paediatrics, Yangpu District Kongjiang Hospital, Shanghai 200093, P.R. China.
Limin ZhongDepartment of Pharmacy, Yangpu District Kongjiang Hospital, Shanghai 200093, P.R. China.
Lei WangDepartment of Rehabilitation, Yangpu District Kongjiang Hospital, Shanghai 200093, P.R. China.
Dongwei GongDepartment of Surgery, Yangpu District Kongjiang Hospital, Shanghai 200093, P.R. China.
Yangpu Hospital of Tongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B virus X (HBX) protein is required for the replication of HBV and plays a role in the progression of hepatitis in humans. However, the underlying function of HBX during HBV‑induced chronic glomerulonephritis (HBV‑GN) is unknown. Echinacoside (ECH) is a phenylethanoid glycoside from the Cistanche genus, which possesses strong antiapoptosis and neuroprotective activities. In the present study, the function of HBX and the relationship between HBX and ECH in human renal tubular epithelial cells (RTECs; HK‑2 cell line) were explored. Reverse transcription‑quantitative PCR and western blot analyses were used to quantify the mRNA and protein expression levels of HBX in HK‑2 cells, respectively. The Cell Counting Kit‑8 assay was performed to analyse cell proliferation. Flow cytometry analysis was used to determine the rate of apoptosis. HBX showed antiproliferative and proapoptotic effects in HK‑2 cells and was positively associated with triggering receptor expressed on myeloid cells 2 (TREM2) expression. Furthermore, ECH disrupted the function of HBX in HK‑2 cells, functioning as an HBX suppressor. Moreover, a specific NF‑κB inhibitor, PDTC, was used to further examine the relationship between HBX and NF‑κB. The results suggested that NF‑κB was involved in the HBX/TREM2 signaling pathway and negatively regulated TREM2 expression in RTECs. The present study provided novel insights into the function of HBX, and also indicated the potential value of ECH as a therapeutic agent for HBV‑GN.

Indexed as

Signal TransductionTrans-ActivatorsViral Regulatory and Accessory ProteinsCell LineCell ProliferationCistancheEpithelial CellsGlycosidesHumansKidney TubulesMembrane GlycoproteinsNF-kappa BReceptors, ImmunologicechinacosideGlycosideshepatitis B virus X proteinMembrane GlycoproteinsNF-kappa BReceptors, ImmunologicTrans-ActivatorsTREM2 protein, humanViral Regulatory and Accessory ProteinsechinacosideHBV-Gnhepatitis B virus XnF-κBTreM2

Identifiers

PMID32626964
PMCPMC7339676
OpenAlexW3032985634

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.