# Calumenin, A Calcium‐Binding Modulatory Protein, Effective in Pathological Calcifications and Cancers, With Therapeutic Application Promise

**Authors:** Parinaz Nasri Nasrabadi, Babak Jahangiri, Zahra Amiri, Forouzandeh Mahjoubi, Fatemeh Masoumi, Alireza Zomorodipour

PMC · DOI: 10.1096/fba.2025-00106 · FASEB BioAdvances · 2025-10-13

## TL;DR

Calumenin is a calcium-binding protein involved in calcium balance, disease processes, and cancer, with potential therapeutic applications.

## Contribution

This paper reviews CALU's diverse roles in calcium homeostasis, disease, and cancer, highlighting its potential as a therapeutic target.

## Key findings

- CALU is involved in calcium homeostasis and pathological calcifications.
- CALU influences cancer through γ-carboxylation of vitamin K-dependent proteins.
- CALU isoforms may balance cellular functions and influence cancer progression.

## Abstract

Calumenin (CALU), a multifunctional E‐F‐hand protein of the CREC family involved in various cellular processes, is ubiquitously expressed in almost all human tissues, although its expression level is tissue‐specific. CALU plays an effective role in calcium (Ca) homeostasis throughout various Ca2+‐related processes, and its correlations with various ER‐related functions are evident. Due to its propensity to bind Ca, participation in calcium ion (Ca2+)‐dependent activities, major cellular processes, such as the production and maintenance of extracellular matrix, have been attributed to this multifaceted protein. In this regard, CALU's association with various normal calcification processes, as well as pathologic Ca deposits, is apparent. Additionally, its key role as a crossroads among various normal cellular processes and many inflammatory diseases and cancers is also evident. The important correlation of CALU with cancer‐related proteins through its regulatory role in γ‐carboxylation of known cancer‐related vitamin K‐dependent proteins has also been noted. The opposing and pleiotropic functions of the CALU isoforms might play balancing roles in establishing a state of equilibrium in the cell. Given the contradictory functions of CALU isoforms during cancer, the need for a balance between these isoforms, as well as the existence of mechanisms to regulate their ratio in normal cells, is speculated. The relationship between CALU and immune response, tumor‐infiltrating immune cells, and cancer patients' responsiveness to various cancer therapies is also described. In this regard, the involvement of the CALU isoform in response to cancer treatment and various immune pathways is discussed. This comprehensive review addresses the outstanding features and the latest findings on CALU's molecular aspects and diverse functions in various physiological processes and pathological conditions.

Calumenin (CALU) is effective in calcium homeostasis, involved in various cellular processes, ER‐related functions, normal calcification processes, pathological calcium deposits, inflammatory diseases, and cancers. Additionally, it has been linked to cancer by controlling the γ‐carboxylation of vitamin K‐dependent proteins linked to cancer. The conflicting functions of its isoforms point to its significance in maintaining cellular state of equilibrium. The association of CALU and immune response, tumor‐infiltrating immune cells, and response to various cancer therapies has also been speculated.

## Linked entities

- **Genes:** CALU (calumenin) [NCBI Gene 813]
- **Proteins:** calumenin (calumenin homologue), CALU (calumenin)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** CALU (calumenin) [NCBI Gene 813], PROS1 (protein S) [NCBI Gene 5627] {aka PROS, PS21, PS22, PS23, PS24, PS25}
- **Diseases:** Cancers (MESH:D009369), inflammatory diseases (MESH:D007249), calcification (MESH:D002114)
- **Chemicals:** Ca2+ (-), Ca (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12516920/full.md

## References

286 references — full list in the complete paper: https://tomesphere.com/paper/PMC12516920/full.md

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Source: https://tomesphere.com/paper/PMC12516920