Evidence mapPaperPMID 42414743Full record

ReviewCardiovascular toxicology2026

Calcium and TRPML-Mediated Autophagy: Implications in Cancer, Cardiovascular Diseases, and Cardio-Oncology.

Joseph Adu-Amankwaah, Vincent Kawuribi, Manuella Quaye, Ling Sha, Siwen Fan, Prakriti Kaur, Vishal Sharma, Osinachi Uchechi Okpoko, Zeyuan Yin

Abstract readReview
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In one paragraph

Review in Cardiovascular toxicology, 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

9 authors.

Joseph Adu-Amankwaah *Department of Physiology, School of Basic Medicine, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China. amankwaahj@ymail.com.
Vincent Kawuribi *Department of Biomedical Engineering, School of Medical Imaging, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Manuella QuayeDepartment of Physiology, School of Basic Medicine, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Ling ShaSchool of Clinical Medicine, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Siwen FanJiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Prakriti KaurSchool of International Education, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Vishal SharmaSchool of International Education, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Osinachi Uchechi OkpokoSchool of International Education, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China.
Zeyuan YinThe First Clinical Medical School, Xuzhou Medical University, Xuzhou, 221006, Jiangsu Province, China. zeyuan.yin@xzhmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is an essential cellular process that maintains homeostasis, regulates organelle turnover, preserves energy balance, and ensures protein quality control. Central to autophagy regulation is calcium (Ca²⁺) signaling, which integrates inputs from multiple Ca²⁺ channels and handling proteins, including L-type and T-type voltage-gated Ca²⁺ channels, transient receptor potential mucolipin (TRPML) channels, inositol 1,4,5-trisphosphate receptors (IP3Rs), ryanodine receptors (RyRs), the mitochondrial calcium uniporter (MCU), sodium-calcium exchangers (NCX), sarco/endoplasmic reticulum Ca²⁺-ATPase (SERCA), and calcium/calmodulin-dependent protein kinase II (CaMKII). Although these regulators are well studied, their disease-specific functions remain context-dependent and complex. In cancer, Ca²⁺-regulated autophagy enhances metabolic flexibility, maintains mitochondrial integrity, promotes resistance to chemotherapy, and facilitates immune evasion, thereby supporting tumor growth and survival. Conversely, in cardiovascular diseases (CVDs), autophagy enables cardiomyocytes to adapt to ischemic, inflammatory, and hemodynamic stress. However, dysregulated Ca²⁺ signaling and impaired autophagic flux contribute to tumor progression and pathological cardiac remodeling, respectively. This review explores the molecular mechanisms underlying Ca²⁺-dependent autophagy in cancer and CVDs, providing a detailed analysis of shared signaling pathways and potential therapeutic targets. Discussed in this review, the emerging field of cardio-oncology highlights a mechanistic convergence in which anticancer therapies disrupt cardiomyocyte Ca²⁺ homeostasis, causing mitochondrial Ca²⁺ overload, ER stress, and defective autophagy, ultimately leading to cardiotoxicity, while tumor cells exploit the same pathways to survive therapeutic stress. By elucidating the spatiotemporal dynamics of Ca²⁺ signaling and autophagy, we identify common molecular hubs and propose precision strategies to enhance anticancer efficacy while preserving cardiac function, advancing translational innovation in cardio-oncology.

Indexed as

AutophagyCalciumCalcium SignalingCardiovascular DiseasesMyocytes, CardiacNeoplasmsTransient Receptor Potential ChannelsAnimalsAntineoplastic AgentsCardiotoxicityHumansAntineoplastic AgentsCalciumTransient Receptor Potential ChannelsAutophagyCalcium signalingCancer therapy–induced cardiotoxicityCardio-oncologyTRPML1

Identifiers

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.