Evidence map›Paper›PMID 31379569›Full record

ReviewFrontiers in pharmacology2019

Metacaspases: Potential Drug Target Against Protozoan Parasites.

Vandana, Rajnikant Dixit, Rajnarayan Tiwari, Anju Katyal, Kailash C Pandey

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. An inclusive assessment of apoptosis mechanisms inCurrent research in parasitology & vector-borne diseases · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Dissecting The role ofEmerging microbes & infections · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Mediterranean Diet: Lipids, Inflammation, and Malaria Infection.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Withanolides fromPathogens (Basel, Switzerland) · 2019
    Article
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

5 authors at 3 institutions in 1 country.

VandanaHost-Parasite Interaction Biology Group, ICMR-National Institute of Malaria Research, New Delhi, India.
Rajnikant DixitHost-Parasite Interaction Biology Group, ICMR-National Institute of Malaria Research, New Delhi, India.
Rajnarayan TiwariDepartment of Biochemistry, ICMR-National Institute for Research in Environmental Health, Bhopal, India.
Anju KatyalDr Ambedkar Center for Biomedical Research, Delhi University, New Delhi, India.
Kailash C PandeyHost-Parasite Interaction Biology Group, ICMR-National Institute of Malaria Research, New Delhi, India.
Ambedkar University Delhi · INNational Institute of Malaria Research · INICMR National Institute for Research in Environmental Health

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the numerous strategies/targets for controlling infectious diseases, parasites-derived proteases receive prime attention due to their essential contribution to parasite growth and development. Parasites produce a broad array of proteases, which are required for parasite entry/invasion, modification/degradation of host proteins for their nourishment, and activation of inflammation that ensures their survival to maintain infection. Presently, extensive research is focused on unique proteases termed as "metacaspases" (MCAs) in relation to their versatile functions in plants and non-metazoans. Such unique MCAs proteases could be considered as a potential drug target against parasites due to their absence in the human host. MCAs are cysteine proteases, having Cys-His catalytic dyad present in fungi, protozoa, and plants. Studies so far indicated that MCAs are broadly associated with apoptosis-like cell death, growth, and stress regulation in different protozoa. The present review comprises the important research outcomes from our group and published literature, showing the variable properties and function of MCAs for therapeutic purpose against infectious diseases.

Indexed as

druggable targetmalariametacaspasesplasmodiumproteases

Identifiers

PMID31379569
PMCPMC6657590
OpenAlexW2953028643

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.