Tenascin-C: an emerging prognostic biomarker in diabetes
Editorial Commentary

Tenascin-C: an emerging prognostic biomarker in diabetes

Saori Yonebayashi#, Kazuko Tajiri#, Siqi Li, Akira Sato

Department of Cardiology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan

#These authors contributed equally to this work.

Correspondence to: Akira Sato, MD, PhD. Department of Cardiology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan. Email: asato@md.tsukuba.ac.jp.

Comment on: Gellen B, Thorin-Trescases N, Thorin E, et al. Serum tenascin-C is independently associated with increased major adverse cardiovascular events and death in individuals with type 2 diabetes: a French prospective cohort. Diabetologia 2020;63:915-23.


Submitted Jun 04, 2020. Accepted for publication Jun 17, 2020.

doi: 10.21037/atm-2020-116


Diabetes has become one of the most pressing issues in the last few decades. The worldwide prevalence of diabetes has reached 380 million (1). Furthermore, cardiovascular disease (CVD) is the leading cause of death in diabetes patients (2). Therefore, cardiovascular (CV) risk stratification is particularly important in diabetics and the search for new predictive biomarkers of CV disease is critical to find. A recent issue of Diabetologia, Gellen et al. (3) showed the association of serum concentration of tenascin-C (TNC), an extracellular matrix (ECM) glycoprotein, with all-cause mortality and major adverse CV events (MACE). The investigators measured serum TNC concentrations from 1,321 type 2 diabetes patients and monitored them for 89 months. They reported that TNC concentrations were independently correlated with a higher risk of all-cause death and MACE [composed of CV death, non-fatal myocardial infarction (MI), and non-fatal stroke]. Using TNC concentrations in addition to conventional risk factors, the prediction of the all-cause death and MACE risk improved modestly, but significantly.

TNC is a non-structural ECM expressed in the heart’s early embryonic development, but it is not present in the normal adult myocardium (4). In tissue injury or active remodeling, its expression increases rapidly in a spatiotemporally restricted manner (4). It has a broad range of effects which include cell adhesion, motility, survival, proliferation, and differentiation in tissue morphogenesis and remodeling including the CV system [reviewed in (5,6)]. Recently, TNC is gaining attention as a regulator of inflammation through various molecular mechanisms [reviewed in (7)]. Animal models have greatly advanced our understanding of the molecular mechanisms of TNC involved in CV pathogenesis over the last two decades. Moreover, an increasing number of studies have reported the use of the serum TNC level as a biomarker for assessing disease activity and predicting the prognosis of patients with CVDs.

We previously reported that serum TNC concentrations were elevated in patients following acute MI and remained higher in patients with adverse ventricular remodeling (8). We also reported that serum TNC levels measured in patients on day 5 after admission for acute MI has a similar prognostic value to that of plasma BNP levels (9). Moreover, the combination of serum TNC and plasma BNP levels with established prognostic markers improved risk stratification for MACE and cardiac death (9). In the acute inflammatory phase of MI, TNC is exclusively localized in the border zone between intact myocardium and infarcted lesion, but becomes absent in the scar-formation stage (10-12). In our present study, TNC knockout (KO) mice were protected from ventricular adverse remodeling, with decreased inflammatory M1- and increased regulatory M2-macrophage infiltration detected in the TNC KO heart during the acute phase after MI (12). In vitro experiments showed that TNC promoted macrophages to shift to an M1 phenotype via Toll-like receptor 4, whereas under M2-altering conditions, TNC suppressed interferon regulatory factor 4 expression, resulting in inhibition of M2 polarization (12). Thus, it has been suggested that TNC accelerates adverse post-infarction remodeling by perturbing macrophage functions.

Several clinical studies have demonstrated the potential use of TNC for pathological evaluation and prognosis assessment in patients with heart failure (13,14). In one study, cardiac pressure overload induced marked induction and interstitial deposition of TNC, which accelerated fibrosis, hypertrophy, and dysfunction in failing hearts (15,16). In another study, the local production of TNC acted as a trigger for monocyte/macrophage recruitment and shifted them into a pro-inflammatory phenotype that exacerbated cardiac dysfunction (16,17). In a model of myocarditis, we have previously shown that TNC worsens autoimmune myocarditis by inducing dendritic cell activation and T-helper 17 cell differentiation via Toll-like receptor 4 (18). Thus, these results suggest that TNC may act as an endogenous driver of innate immunity in the failing heart.

TNC has also been reported to be involved in the pathophysiology of aneurysmal and dissecting aortic lesions. In human and CaCl2-induced mouse abdominal aortic aneurisms, TNC expression levels were positively correlated with the expansion rate of the aneurismal diameter and the destruction of the aortic wall (19). However, in a mouse model of aortic stiffening, a known risk factor for acute aortic dissection, TNC protects the aorta from dissection, but not from aneurysmal formation and works as a stress-induced molecular inhibitor to maintain the aortic integrity under acute stress (20). We have previously reported that high serum TNC levels on admission is a predictor of high mortality within 30 days (21), whereas high serum TNC levels at 7 days after admission predicts a low risk of aortic enlargement during the chronic stage (22). These clinical data suggest that the role of TNC in the aorta is complex and alters depending on the state of the aorta that changes as time proceeds after aortic dissection. Further studies are needed to clarify the exact role of TNC in the progression of acute aortic dissection.

In the cohort study from Gellen et al. (3), higher TNC concentrations were associated with longer durations of diabetes. However, whether elevated TNC levels are a cause or a result of diabetes is still unknown. One possibility is that TNC directly activates signaling pathways that lead to diabetes. Alternatively, it is also possible that diabetic conditions could increase the amount of TNC. Finally, the defining question as to whether TNC is beneficial or detrimental in diabetes still remains unanswered. Further investigations are necessary to elucidate the potential role of TNC in diabetes as an etiological factor.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Annals of Translational Medicine. The article did not undergo external peer review.

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure from (available at http://dx.doi.org/10.21037/atm-2020-116). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


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Cite this article as: Yonebayashi S, Tajiri K, Li S, Sato A. Tenascin-C: an emerging prognostic biomarker in diabetes. Ann Transl Med 2020;8(24):1699. doi: 10.21037/atm-2020-116