Evidence mapPaperPMID 42433657Full record

ReviewOpen medicine (Warsaw, Poland)2026

SMP30: a promising cancer biomarker with therapeutic potential.

Pei Chen, Yu-Ling Zhang, Ying Guo

Abstract readReview
In one paragraph

Review in Open medicine (Warsaw, Poland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Pei ChenDepartment of Basic Medicine, Jiangsu College of Nursing, Huai'an, China.ORCID https://orcid.org/0000-0002-5763-7390
Yu-Ling ZhangDepartment of Basic Medicine, Jiangsu College of Nursing, Huai'an, China.
Ying GuoDepartment of Clinical Laboratory, Huai'an Maternal and Child Health Care Hospital, Huai'an, China.ORCID https://orcid.org/0009-0009-9754-0655

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: SMP30 is a calcium binding protein closely related to cellular senescence. Low expression of SMP30 is significantly associated with malignant progression and poor prognosis in tumors, suggesting it values as a potential diagnostic biomarker and therapeutic target. Content: We systematically review recent studies on SMP30 in human tumors, highlight its role in modulating tumor cells proliferation and apoptosis, and detail mechanism of its involvement in glycolipid metabolic reprogramming as well as its impact on the tumor microenvironment and metastasis. Summary: SMP30 is involved in regulating cell cycle, maintaining intracellular homeostasis, and protecting cells from external damage. It supports cellular homeostasis and resistance to apoptosis by modulating intracellular Ca Outlook: SMP30 is a key regulator of cellular senescence with significant implication in tumorigenesis. Low expression of SMP30 relates to multiple oncogenic mechanisms, including cell cycle, apoptosis, metabolic reprogramming, epithelial mesenchymal transition (EMT), and immune evasion, which shows promising potential for early diagnosis, prognostic evaluation, and targeted therapy of cancers.

Indexed as

Ca2+ homeostasiscellular senescenceSASPSMP30therapeutic target

Identifiers

PMID42433657
PMCPMC13351293

What Socratic 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 Socratic graph.