Evidence map›Paper›PMID 35036051›Full record

ArticleMolecular therapy. Nucleic acids2022

DRAM1 increases the secretion of PKM2-enriched EVs from hepatocytes to promote macrophage activation and disease progression in ALD.

Jie Tan, Jie Zhang, Mengke Wang, Yifen Wang, Mengzhen Dong, Xuefeng Ma, Baokai Sun, Shousheng Liu, Zhenzhen Zhao, Lizhen Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. PKM2: A gatekeeper in macrophage metabolic reprogramming.Journal of pharmaceutical analysis · 2026
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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 2 institutions in 1 country.

Jie TanDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Jie ZhangDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Mengke WangDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Yifen WangDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Mengzhen DongDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Xuefeng MaDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Baokai SunDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Shousheng LiuClinical Research Center, Qingdao Municipal Hospital, Qingdao University, Qingdao 266071, China.
Zhenzhen ZhaoClinical Research Center, Qingdao Municipal Hospital, Qingdao University, Qingdao 266071, China.
Lizhen ChenDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Wenwen JinDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Kai LiuBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing 100069, China.
Yongning XinDepartment of Infectious Diseases, Qingdao Municipal Hospital, Qingdao University, Qingdao 266011, China.
Likun ZhuangClinical Research Center, Qingdao Municipal Hospital, Qingdao University, Qingdao 266071, China.
Qingdao University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA damage-regulated autophagy modulator 1 (DRAM1) could play important roles in inflammation and hepatic apoptosis, while its roles in alcohol-related liver disease (ALD), which is characterized by hepatic inflammation and apoptosis, are still unclear. In this study, we explored the expression, role, and mechanism of DRAM1 in ALD. Firstly, our results showed that DRAM1 was significantly increased in liver tissues of mice at the early stage of alcohol treatment. In addition, DRAM1 knockout reduced, and liver-specific overexpression of DRAM1 aggravated, alcohol-induced hepatic steatosis, injury, and expressions of M1 macrophage markers in mice. Furthermore, ethanol-induced DRAM1 of hepatic cells increased pyruvate kinase M2 (PKM2)-enriched extracellular vesicles (EVs), and ectosomes derived from hepatic cells with DRAM1 overexpression promoted macrophage activation. Mechanistic investigations showed that DRAM1 interacted with PKM2 and increased the PKM2 level in plasma membrane. At last, DRAM1 was significantly increased in liver tissues of ALD patients, and it was positively correlated with M1 macrophage markers. Taken together, this study revealed that ethanol-induced DRAM1 of hepatic cells could increase the PKM2-enriched EVs, promote macrophage activation, and aggravate the disease progression of ALD. These findings suggested that DRAM1 might be a potentially promising target for the therapy of ALD.

Indexed as

Alcohol-related liver diseaseDRAM1Extracellular vesiclesMacrophage activationPKM2

Identifiers

PMID35036051
PMCPMC8728309
OpenAlexW4200349218

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.