Evidence map›Paper›PMID 28074340›Full record

ArticleMolecular and cellular biochemistry2017

Clinical significance of cathepsin L and cathepsin B in dilated cardiomyopathy.

Siddharth Mehra, Manish Kumar, Mansi Manchanda, Ratnakar Singh, Bhaskar Thakur, Neha Rani, Sudheer Arava, Rajiv Narang, Dharamvir Singh Arya, Shyam S Chauhan

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 33% of its field
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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cathepsins in Neurological Diseases.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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

10 authors at 1 institution in 1 country.

Siddharth MehraDepartment of Biochemistry, All India Institute of Medical Sciences, Room No. 3009, New Delhi, 110029, India.
Manish KumarDepartment of Biochemistry, All India Institute of Medical Sciences, Room No. 3009, New Delhi, 110029, India.
Mansi ManchandaDepartment of Biochemistry, All India Institute of Medical Sciences, Room No. 3009, New Delhi, 110029, India.
Ratnakar SinghDepartment of Biochemistry, All India Institute of Medical Sciences, Room No. 3009, New Delhi, 110029, India.
Bhaskar ThakurDepartment of Biostastics, All India Institute of Medical Sciences, New Delhi, India.
Neha RaniDepartment of Pharmacology, All India Institute of Medical Sciences, New Delhi, India.
Sudheer AravaDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Rajiv NarangDepartment of Cardiology, All India Institute of Medical Sciences, New Delhi, India.
Dharamvir Singh AryaDepartment of Pharmacology, All India Institute of Medical Sciences, New Delhi, India.
Shyam S ChauhanDepartment of Biochemistry, All India Institute of Medical Sciences, Room No. 3009, New Delhi, 110029, India. s_s_chauhan@hotmail.com.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulated expression of lysosomal cysteine cathepsins is associated with adverse cardiac remodeling, a characteristic of several cardiovascular diseases. However, the information regarding the role of cysteine cathepsin L (CTSL) and cathepsin B (CTSB) in dilated cardiomyopathy (DCM) is limited. The present study was aimed to investigate the expression of CTSL and CTSB in animal model of doxorubicin (doxo)-induced cardiomyopathy as well as in peripheral blood samples of DCM patients. Cardiac tissue sections from doxo-treated and control rats were used to study the expression of CTSL and CTSB by enzyme assay and immunohistochemistry (IHC). Peripheral blood mononuclear cells (PBMCs) isolated from DCM patients (n = 29) along with age-matched healthy controls (n = 28) were used to assay enzymatic activity of these cathepsins. Activities of these proteases were further correlated with echocardiographic parameters of DCM patients. A significant increase in CTSL activity and protein expression was observed with no changes in CTSB levels in doxo-treated rats as compared to controls. We also observed a drastic increase in the functional activity of cathepsin L+cathepsin B (CTSL+B), CTSL, and CTSB in DCM patients compared to controls (p ≤ 0.001). Increased levels of these proteases exhibited a statistically significant correlation with reduced left ventricular ejection fraction (LVEF) in DCM patients (ρ = -0.58, p = 0.01). For the first time, this study demonstrates a correlation between increased expression of CTSL and CTSB in PBMCs with severity of left ventricular dysfunction in DCM patients. Thus, these proteases may serve as blood-based biomarker of DCM and prove useful in its management.

Indexed as

AdultAnimalsBiomarkersCardiomyopathy, DilatedCathepsin BCathepsin LDisease Models, AnimalDoxorubicinEchocardiographyFemaleHeart VentriclesHumansMaleMiddle AgedRatsStroke VolumeBiomarkersCathepsin BCathepsin LCTSB protein, humanCTSL protein, humanDoxorubicinCathepsin BCathepsin LDilated cardiomyopathyDoxorubicinExtracellular matrix and cardiac remodelingPBMCs

Identifiers

PMID28074340
OpenAlexW2569947718

What OpenQuestion 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 OpenQuestion graph.