Evidence map›Paper›PMID 32592353›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2020

Natural Killer Cells Expanded and Preactivated Exhibit Enhanced Antitumor Activity against Different Tumor Cells in Vitro.

Biplob Kumar Biswas, Sameer Ahmad Guru, Mamta Pervin Sumi, Elvia Jamatia, Rohit Kumar Gupta, Pramod Lali, Bidhan Chandra Konar, Alpana Saxena, Rashid Mir

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. FLT3L Release by Natural Killer Cells Enhances Response to Radioimmunotherapy in Preclinical Models of HNSCC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  2. Effects of Wild Yam Root (Cancer genomics & proteomics
    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

9 authors at 1 institution in 1 country.

Biplob Kumar BiswasDepartment of Biochemistry, Maulana Azad Medical College (MAMC) and Associated Hospitals, New Delhi, India.
Sameer Ahmad GuruMultidisciplinary Research Unit (MRU), Maulana Azad Medical College and Associated Hospitals, Bahadur Shah Zafar Marg, New Delhi, 110002, India.
Mamta Pervin SumiDepartment of Gastroinstestinal Surgery G B Pant Postgraduate Institute of Medical Education and Research (GIPMER), New Delhi, India.
Elvia JamatiaDepartment of Biochemistry, Maulana Azad Medical College (MAMC) and Associated Hospitals, New Delhi, India.
Rohit Kumar GuptaDepartment of Biochemistry, Maulana Azad Medical College (MAMC) and Associated Hospitals, New Delhi, India.
Pramod LaliDepartment of Biochemistry, Maulana Azad Medical College (MAMC) and Associated Hospitals, New Delhi, India.
Bidhan Chandra KonarDepartment of Biochemistry, Maulana Azad Medical College (MAMC) and Associated Hospitals, New Delhi, India.
Alpana SaxenaDepartment of Biochemistry, Maulana Azad Medical College (MAMC) and Associated Hospitals, New Delhi, India.
Rashid MirDepartment of Medical Lab Technology, Faculty of Applied Medical Sciences, Prince Fahd Bin Sultan Research chair, University of Tabuk, Saudi Arabia.
Maulana Azad Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the emerging treatment strategies for cancer particularly for haematological malignancies is natural killer (NK) cell therapy. However, the availability of a best approach to maximize NK cell anticancer potential is still awaited. It is well established that cytokine-induced memory-like NK cells have the potential to differentiate after a short period of preactivation with interleukins-IL-12, IL-15, and IL-18 and exhibit increased responses to cytokine or activating receptor restimulation for weeks to months after preactivation. We demonstrated that NK cells differentiated from CD34+ cells isolated from cord blood show increased antitumor potential in vitro against different cancer cells. Using flow cytometry, we found that NK cells were able to induce apoptosis in cancer cells in vitro. We further analysed surviving gene expression by quantitative real time PCR and reported that NK cells cause down regulation of survivin gene expression in tumor cells. Therefore, NK cell therapy represents a promising immunotherapy for cancers like AML and other haematological malignancies. It concluded that NK cells can be differentiated from CD34+ cells isolated from cord blood ,are able to induce apoptosis and induce increased antitumor potential in vitro against different cancer cells besides cause downregulation of survivin gene expression in tumor cells. Therefore, NK cell therapy represents a promising immunotherapy for different cancer types and haematological malignancies. Furthers studies are necessary to confirm our findings.<br />.

Indexed as

Cell DifferentiationCell ProliferationCells, CulturedCytotoxicity, ImmunologicFetal BloodHumansInterferon-gammaInterleukin-12Interleukin-15Interleukin-18In Vitro TechniquesKiller Cells, NaturalLymphocyte ActivationNeoplasmsIL15 protein, humanIL18 protein, humanInterferon-gammaInterleukin-12Interleukin-15Interleukin-18CD34+ cellsK562 (Chronic Myeloid Leukaemia)Natural killer (NK)T47D (Human Breast Adenocarcinoma)Umbilical Cord Blood (UCB)

Identifiers

PMID32592353
PMCPMC7568895
OpenAlexW3037042043

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.