Evidence map›Paper›PMID 36918700›Full record

ArticleThe pharmacogenomics journal2023

The expression level of Neuronal Calcium Sensor 1 can predict the prognosis of cytogenetically normal AML.

Weilong Zhang, Jing Wang, Wei Li, Xiaoni Liu, Yali Zhao, Ping Yang, Mingxia Zhu, Kai Hu, Shaoxiang Li, Gehong Dong and 4 more

Abstract read
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In one paragraph

Article in The pharmacogenomics journal, 2023. 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
0.6field-weighted citation impact, top 29% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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 4 institutions in 1 country.

Weilong Zhang *Department of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China.
Jing Wang *Department of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China.
Wei Li *Department of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China.
Xiaoni LiuDepartment of Respiratory Medicine, The First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, China.
Yali ZhaoGeneral Practice Medicine, The First People's Hospital of Huzhou, Huzhou, 313000, China.
Ping YangDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China.
Mingxia ZhuDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China.
Kai HuDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China.
Shaoxiang LiDepartment of Pathology, Beijing Tiantan Hospital Affiliated with Capital Medical University, 100050, Beijing, China.
Gehong DongDepartment of Pathology, Beijing Tiantan Hospital Affiliated with Capital Medical University, 100050, Beijing, China.
Changjian YanDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China. yanchangjian2019@126.com.
Xue HeDepartment of Pathology, Beijing Tiantan Hospital Affiliated with Capital Medical University, 100050, Beijing, China. hexue8@163.com.ORCID 0000-0003-4448-5399
Xiuru ZhangDepartment of Pathology, Beijing Tiantan Hospital Affiliated with Capital Medical University, 100050, Beijing, China. zhangxiuru999@163.com.
Hongmei JingDepartment of Hematology, Lymphoma Research Center, Peking University Third Hospital, 100191, Beijing, China. drjinghm@163.com.ORCID 0009-0002-7352-3964
Peking University · CNCapital Medical University · CNFirst Affiliated Hospital of Gannan Medical University · CNThird People's Hospital of Huzhou · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is malignant clonal expansion of myeloid blasts with high heterogeneity and numerous molecular biomarkers have been found to judge the prognosis in some specific classifications of AML. Furthermore, as for patients with cytogenetically normal acute myeloid leukemia (CN-AML), we need to find more new biomarkers to predict the patients' outcomes. Recently, the expression level of Neuronal Calcium Sensor 1 (NCS1) has been associated with the prognosis of breast cancer and hepatocellular carcinoma, but nothing related has been reported about hematological malignancies. Therefore, we make this study to explore the relationship between the NCS1 expression level and CN-AML. We analyzed the relation between survival and NCS1 RNA expression through 75 CN-AML patients from Cancer Genome Atlas (TCGA) database and 433 CN-AML patients (3 independent datasets) from Gene Expression Omnibus (GEO) database. Additionally, we compared the NCS1 RNA expression between 138 leukemia stem cells positive (LSCs+) samples and 89 leukemia stem cells negative (LSCs-) samples from 78 AML patients from GSE76004 dataset. In our study, CN-AML patients with high expression level of NCS1 have longer EFS or OS. In addition, the NCS1 expression level in leukemia stem cells was low (p = 0.00039). According to these findings, we concluded that the high expression of NCS1 can predict favorable prognosis in CN-AML patients. Furthermore, our work put forward that NCS1 expresses lower in LSCs+, which might be an important mechanism to explain the aggressiveness of AML.

Indexed as

Leukemia, Myeloid, AcuteHumansNeuronal Calcium-Sensor ProteinsNeuropeptidesRNAfrequenin calcium sensor proteinsNeuronal Calcium-Sensor ProteinsNeuropeptidesRNA

Identifiers

PMID36918700
OpenAlexW4324150541

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Registered trials

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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.