Key result
Massive rotator cuff tears linked to ~2-fold upregulation of supraspinatus CAPN1, UBE2B, and UBE3A transcripts.
Why the study?
The relationship between expression of atrophy-related mRNA and tendon tear size in supraspinatus muscle was unclear.
Are mRNA transcripts of atrophy-related genes overexpressed in the supraspinatus muscle of patients with rotator cuff tears compared to those without?
Observational (n=59)
Are mRNA transcripts of atrophy-related genes overexpressed in the supraspinatus muscle of patients with rotator cuff tears compared to those without?
Effect estimate: >2-fold upregulation
Upregulation of specific atrophy-related genes (CAPN1, UBE2B, UBE3A) in massive rotator cuff tears suggests their involvement in muscle atrophy and potential impairment of functional recovery after surgical repair.
May implicate these genes in massive tear-related atrophy; hypothesis-generating for targeted therapies, pending prospective validation.
Skeletal muscle atrophy and fatty infiltration develop after tendon tearing. The extent of atrophy serves as one prognostic factor for the outcome of surgical repair of rotator cuff tendon tears. We asked whether mRNA of genes involved in regulation of degradative processes leading to muscle atrophy, ie, FOXOs, MSTN, calpains, cathepsins, and transcripts of the ubiquitin-proteasome pathway, are overexpressed in the supraspinatus muscle in patients with and without rotator cuff tears. We evaluated biopsy specimens collected during surgery of 53 consecutive patients with different sizes of rotator cuff tendon tears and six without tears. The levels of corresponding gene transcripts in total RNA extracts were assessed by semiquantitative reverse transcriptase-polymerase chain reaction (RT-PCR) analysis. Supraspinatus muscle atrophy was assessed by MRI. The area of muscle tissue (or atrophy), decreased (increased) with increasing tendon tear size. The transcripts of CAPN1, UBE2B, and UBE3A were upregulated more than twofold in massive rotator cuff tears as opposed to smaller tears or patients without tears. These atrophy gene products may be involved in cellular processes that impair functional recovery of affected muscles after surgical rotator cuff repair. However, the damaging effects of gene products in their respective proteolytic processes on muscle structures and proteins remains to be investigated.
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Schmutz et al. (2008) conducted an observational in Rotator cuff tendon tears (n=59). Massive rotator cuff tears vs. Smaller tears or no tears was evaluated on Expression levels of atrophy gene transcripts (CAPN1, UBE2B, UBE3A) (>2-fold upregulation). Massive rotator cuff tears were associated with a more than twofold upregulation of CAPN1, UBE2B, and UBE3A transcripts in the supraspinatus muscle compared to smaller or no tears.
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