Evidence map›Paper›PMID 36438839›Full record

ReviewFrontiers in pharmacology2022

The lysosome as a novel therapeutic target of EGFR-mediated tumor inflammation.

Woo Jung Sung, Dohyang Kim, Anlin Zhu, Namki Cho, Hee Min Yoo, Ji Heon Noh, Kyoung Mi Kim, Hyun-Su Lee, Jaewoo Hong

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. SMURF2 in Anticancer Therapy: Dual Role in Carcinogenesis and Theranostics.International journal of molecular sciences · 2026
    Review
  3. Review
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 4 institutions in 1 country.

Woo Jung SungDepartment of Pathology, Daegu Catholic University School of Medicine, Daegu, South Korea.
Dohyang KimDepartment of Physiology, Daegu Catholic University School of Medicine, Daegu, South Korea.
Anlin ZhuDepartment of Physiology, Daegu Catholic University School of Medicine, Daegu, South Korea.
Namki ChoCollege of Pharmacy, Chonnam National University, Gwangju, South Korea.
Hee Min YooBiometrology Group, Korea Research Institute of Standards and Science, Daejeon, South Korea.
Ji Heon NohDepartment of Biochemistry, Chungnam National University, Daejeon, South Korea.
Kyoung Mi KimDepartment of Biological Sciences, Chungnam National University, Daejeon, South Korea.
Hyun-Su LeeDepartment of Physiology, Daegu Catholic University School of Medicine, Daegu, South Korea.
Jaewoo HongDepartment of Physiology, Daegu Catholic University School of Medicine, Daegu, South Korea.
Daegu Catholic University · KRChungnam National University · KRChonnam National University · KRKorea University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EGFR-mediated tumors have been targeted to overcome several different malignant cancers. EGFR overexpression and mutations are directly related to the malignancy, which makes the therapy more complicated. One reason for the malignancy is the induction of AP1 followed by inflammation

Indexed as

combination therapyEGFRErbBlysosomeTKI

Identifiers

PMID36438839
PMCPMC9691834
OpenAlexW4308802128

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.