Evidence map›Paper›PMID 33983572›Full record

ReviewAdvances in experimental medicine and biology2021

Phospholipase Signaling in Breast Cancer.

Yu Jin Lee, Kyeong Jin Shin, Hyun-Jun Jang, Dong-Young Noh, Sung Ho Ryu, Pann-Ghill Suh

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Insights Into circRNA-Mediated Lipid Metabolism in Cancer Progression.Journal of cellular and molecular medicine · 2026
    Review
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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

6 authors at 3 institutions in 1 country.

Yu Jin LeeSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Kyeong Jin ShinSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Hyun-Jun JangSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Dong-Young NohDepartment of Surgery, College of Medicine, Seoul National University, Seoul, South Korea.
Sung Ho RyuDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Pann-Ghill SuhSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea. pgsuh@unist.ac.kr.
Ulsan National Institute of Science and Technology · KRPohang University of Science and Technology · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer progression results from subversion of multiple intra- or intercellular signaling pathways in normal mammary tissues and their microenvironment, which have an impact on cell differentiation, proliferation, migration, and angiogenesis. Phospholipases (PLC, PLD and PLA) are essential mediators of intra- and intercellular signaling. They hydrolyze phospholipids, which are major components of cell membrane that can generate many bioactive lipid mediators, such as diacylglycerol, phosphatidic acid, lysophosphatidic acid, and arachidonic acid. Enzymatic processing of phospholipids by phospholipases converts these molecules into lipid mediators that regulate multiple cellular processes, which in turn can promote breast cancer progression. Thus, dysregulation of phospholipases contributes to a number of human diseases, including cancer. This review describes how phospholipases regulate multiple cancer-associated cellular processes, and the interplay among different phospholipases in breast cancer. A thorough understanding of the breast cancer-associated signaling networks of phospholipases is necessary to determine whether these enzymes are potential targets for innovative therapeutic strategies.

Indexed as

Breast NeoplasmsPhospholipase DHumansPhospholipasesPhospholipidsSignal TransductionTumor MicroenvironmentType C PhospholipasesPhospholipase DPhospholipasesPhospholipidsType C PhospholipasesBreast cancerCell signalingMetastasisPhospholipasesPhospholipidProliferation

Identifiers

PMID33983572
OpenAlexW3162615810

What Socratic holds

Textmetadata
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 Socratic graph.