# Serum Mitochondrial Open Reading Frame of the 12S rRNA-c (MOTS-c) Dynamics as a Complementary Marker of Treatment Response in Newly Diagnosed Multiple Myeloma: A Prospective Analysis

**Authors:** Veysel Erol, Esin Avci, Sibel Kabukcu Hacioglu, Nil Guler, Gulsum Akgun Cagliyan, Başak Ünver Koluman, Ismail Can Kendir, Ozde Elver, Kayihan Kara, Erhan Kaya, Nevin Alayvaz Aslan

PMC · DOI: 10.7759/cureus.98204 · Cureus · 2025-11-30

## TL;DR

This study explores how changes in serum MOTS-c levels may indicate treatment response in newly diagnosed multiple myeloma patients.

## Contribution

The study introduces serum MOTS-c dynamics as a potential complementary marker for assessing treatment response in multiple myeloma.

## Key findings

- Responding patients showed increased MOTS-c levels after treatment, while refractory cases did not.
- Post-treatment MOTS-c levels inversely correlated with changes in calcium and neutrophil counts.
- MOTS-c dynamics may reflect metabolic and microenvironmental adaptations to therapy.

## Abstract

Objectives: This study evaluated whether serum levels of mitochondrial open reading frame of the 12S rRNA-c (MOTS-c) could provide prognostic insights in patients newly diagnosed with multiple myeloma (MM), particularly in relation to therapeutic responsiveness.

Methods: In a prospective analysis involving 29 MM patients, serum MOTS-c concentrations were measured before and after frontline treatment. Associations between MOTS-c fluctuations and clinical-biochemical variables were systematically explored.

Results: Patients who responded to treatment exhibited a substantial post-therapy increase in MOTS-c levels, while refractory cases showed little to no change. Post-treatment MOTS-c values inversely correlated with calcium and neutrophil count changes. Despite limited standalone predictive capacity, MOTS-c dynamics may reflect microenvironmental and metabolic adaptation linked to treatment response.

Conclusions: Changes in serum MOTS-c concentrations following therapy may serve as complementary markers of clinical response in MM. Further validation in larger cohorts is warranted.

## Linked entities

- **Diseases:** multiple myeloma (MONDO:0009693)

## Full-text entities

- **Diseases:** MM (MESH:D009101)
- **Chemicals:** calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12754562/full.md

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Source: https://tomesphere.com/paper/PMC12754562