Evidence map›Paper›PMID 35692083›Full record

ArticleJournal of cellular and molecular medicine2022

Integrated analysis of pivotal biomarker of LSM1, immune cell infiltration and therapeutic drugs in breast cancer.

Yen-Dun Tony Tzeng, Kuan-Hao Tsui, Ling-Ming Tseng, Ming-Feng Hou, Pei-Yi Chu, Jim Jinn-Chyuan Sheu, Chia-Jung Li

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

7 authors at 4 institutions in 1 country.

Yen-Dun Tony TzengDepartment of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Kuan-Hao TsuiDepartment of Obstetrics and Gynecology, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Ling-Ming TsengSchool of Medicine, National Yang-Ming University, Taipei, Taiwan.
Ming-Feng HouDivision of Breast Surgery, Department of Surgery, Center for Cancer Research, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung, Taiwan.
Pei-Yi ChuDepartment of Pathology, Show Chwan Memorial Hospital, Changhua, Taiwan.
Jim Jinn-Chyuan SheuInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan.
Chia-Jung LiDepartment of Obstetrics and Gynecology, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.ORCID 0000-0002-3773-9015
National Sun Yat-sen University · TWChang Bing Show Chwan Memorial Hospital · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

Kaohsiung Veterans General Hospital KSVGH110-142Kaohsiung Veterans General Hospital VGHKS109-106Ministry of Science Technology R.O.C. MOST 109-2314-B-075B-002Ministry of Science Technology R.O.C. MOST 110-2314-B-075B-011Veterans General Hospitals and University System of Taiwan Joint Research Program VGHUST111-G6-2-2
6 · The paper itself

Abstract

The discovery of early diagnosis and prognostic markers for breast cancer can significantly improve survival and reduce mortality. LSM1 is known to be involved in the general process of mRNA degradation in complexes containing LSm subunits, but the molecular and biological functions in breast cancer remain unclear. Here, the expression of LSM1 mRNA in breast cancer was estimated using The Cancer Genome Atlas (TCGA), Oncomine, TIMER and bc-GenExMiner databases. We found that functional LSM1 inactivation caused by mutations and profound deletions predicted poor prognosis in breast cancer (BRCA) patients. LSM1 was highly expressed in both BRCA tissues and cells compared to normal breast tissues/cells. High LSM1 expression is associated with poorer overall survival and disease-free survival. The association between LSM1 and immune infiltration of breast cancer was assessed by TIMER and CIBERSORT algorithms. LSM1 showed a strong correlation with various immune marker sets. Most importantly, pharmacogenetic analysis of BRCA cell lines revealed that LSM1 inactivation was associated with increased sensitivity to refametinib and trametinib. However, both drugs could mimic the effects of LSM1 inhibition and their drug sensitivity was associated with MEK molecules. Therefore, we investigated the clinical application of LSM1 to provide a basis for sensitive diagnosis, prognosis and targeted treatment of breast cancer.

Indexed as

Breast NeoplasmsProto-Oncogene ProteinsRNA-Binding ProteinsBiomarkersFemaleHumansMCF-7 CellsRNA, MessengerRNA StabilityBiomarkersLSM1 protein, humanProto-Oncogene ProteinsRNA-Binding ProteinsRNA, Messengerbreast cancerdiagnosisimmune infiltrationLSM1multi-omics

Identifiers

PMID35692083
PMCPMC9279588
OpenAlexW4282827619

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.