Evidence map›Paper›PMID 41505219›Full record

ArticleJCI insight2026

Phosphoproteomics identification of ERK-dependent activation of Rps6kb1 in cardiac hypertrophy.

Chao Li, Pengfei Zhang, Kai Zhang, Jane A Cook, Weidan Song, Megan Virostek, Lily A Slotabec, Nadiyeh Rouhi, Mohammed Hazari, Michael I Adenawoola and 15 more

Abstract read
In one paragraph

Article in JCI insight, 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

25 authors.

Chao LiDivision of Cardiology, and.
Pengfei ZhangDepartment of Diabetes and Cancer Metabolism, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, USA.
Kai ZhangDepartment of Diabetes and Cancer Metabolism, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, USA.
Jane A CookDivision of Cardiology, and.
Weidan SongDivision of Cardiology, and.
Megan VirostekTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Lily A SlotabecDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Nadiyeh RouhiDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Mohammed HazariTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Michael I AdenawoolaDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Xiaofei LiuState Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, Nanjing Medical University, Nanjing, China.
Hao ZhangState Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, Nanjing Medical University, Nanjing, China.
Guangyu ZhangDivision of Cardiology, and.
Erica L NiewoldDivision of Cardiology, and.
Qinfeng LiDivision of Cardiology, and.
Yong FangDivision of Cardiology, and.
Waleed M ElhelalyDivision of Cardiology, and.
Xue-Nan SunTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Xuejiang GuoState Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, Nanjing Medical University, Nanjing, China.
Andrew LemoffDepartment of Biochemistry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Yingfeng DengDepartment of Diabetes and Cancer Metabolism, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, USA.
Thomas G GilletteDivision of Cardiology, and.
Ji LiDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Philipp E SchererTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Zhao V WangDepartment of Diabetes and Cancer Metabolism, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, USA.

Funding

UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeffrey M Zigman · 2022 to 2026
$7.4M
Integrative role of Rps6kb1 in pathological cardiac remodelingR01HL171309 · NHLBI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI Zhao Wang · 2024 to 2026
$2.5M
NHLBI NIH HHS R01 HL171309NIDDK NIH HHS P30 DK127984
6 · The paper itself

Abstract

Cardiomyocyte growth is tightly controlled by multiple signaling pathways. Identification of master kinases in this process is essential in exploring potential targets for the treatment of pathological cardiac hypertrophy and heart failure. Here we identified the mTOR-independent activation of ribosomal protein S6 kinase b1 (Rps6kb1) during cardiomyocyte growth. By utilizing phosphoproteomics in primary neonatal rat ventricular myocytes, we revealed Rps6kb1 as one of most activated kinases under growth stimulation. We further demonstrated the role of Rps6kb1 phosphorylation in pathological cardiac hypertrophy and heart failure. We showed that the phosphorylation of multiple sites in Rps6kb1, including T367 in the kinase domain and S418/T421/S424 in the C-terminal domain, is not directly regulated by the activity of mTOR but coupled with the activation of the MEK1/ERK axis. In mice, cardiomyocyte-specific deletion of Rps6kb1 significantly inhibited both constitutively active ERK- and pressure overload-induced cardiac hypertrophy. In contrast, cardiomyocyte-specific overexpression of wild-type Rps6kb1, rather than the phosphorylation-defective mutant, elevated cardiac hypertrophy and augmented pressure overload-induced heart failure. In conclusion, our findings reveal that the MEK/ERK axis primes Rps6kb1 activation through phosphorylation of 2 separate domains of Rps6kb1, which may play an essential role in cardiac hypertrophy and heart failure under hemodynamic stress.

Indexed as

CardiomegalyExtracellular Signal-Regulated MAP KinasesMyocytes, CardiacRibosomal Protein S6 Kinases, 70-kDaRibosomal Protein S6 Kinases, 90-kDaAnimalsCells, CulturedHeart FailureMaleMAP Kinase Signaling SystemMicePhosphorylationProteomicsRatsRibosomal Protein S6 KinasesSignal TransductionExtracellular Signal-Regulated MAP KinasesRibosomal Protein S6 KinasesRibosomal Protein S6 Kinases, 70-kDaRibosomal Protein S6 Kinases, 90-kDaRps6kb1 protein, ratTOR Serine-Threonine KinasesCardiologyCardiovascular diseaseCell biologyHeart failureMolecular biology

Identifiers

PMID41505219
PMCPMC12956007

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.