Evidence map›Paper›PMID 32204484›Full record

ArticleCancers2020

Sea Hare Hydrolysate-Induced Reduction of Human Non-Small Cell Lung Cancer Cell Growth through Regulation of Macrophage Polarization and Non-Apoptotic Regulated Cell Death Pathways.

Marie Merci Nyiramana, Soo Buem Cho, Eun-Jin Kim, Min Jun Kim, Ji Hyeon Ryu, Hyun Jae Nam, Nam-Gil Kim, Si-Hyang Park, Yeung Joon Choi, Sang Soo Kang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
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  7. Article
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  13. Review
  14. Article
  15. Pyroptosis: A promising target for lung cancer therapy.Chinese medical journal pulmonary and critical care medicine · 2023
    Review
  16. Article
  17. Molecular mechanisms of pyroptosis and its role in anti-tumor immunity.International journal of biological sciences · 2023
    Review
  18. Article
  19. Aging · 2022
    Article
  20. Drug delivery strategy in hepatocellular carcinoma therapy.Cell communication and signaling : CCS · 2022
    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

15 authors at 3 institutions in 1 country.

Marie Merci NyiramanaDepartment of Physiology and Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.ORCID 0000-0002-0018-8934
Soo Buem ChoDepartment of Radiology, Ewha Womans University Medical Center, Seoul 07804, Korea.ORCID 0000-0001-5762-7064
Eun-Jin KimDepartment of Physiology and Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.
Min Jun KimDepartment of Anatomy, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.
Ji Hyeon RyuDepartment of Physiology and Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.ORCID 0000-0003-0342-3108
Hyun Jae NamDepartment of Medicine, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.
Nam-Gil KimDepartment of Marine Biology and Aquaculture and Institute of Marine Industry, Gyeongsang National University, Tongyeong 53064, Korea.
Si-Hyang ParkSunmarin Biotech, Tongyeong 53064, Korea.
Yeung Joon ChoiDepartment of Seafood Science and Technology and Institute of Marine Industry, Gyeongsang National University, Tongyeong 53064, Korea.
Sang Soo KangDepartment of Anatomy, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.ORCID 0000-0001-9424-2067
Myunghwan JungDepartment of Microbiology, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.ORCID 0000-0001-8124-8945
Min-Kyoung ShinDepartment of Microbiology, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.ORCID 0000-0003-1782-5351
Jaehee HanDepartment of Physiology and Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.
In-Seok JangDepartment of Thoracic and Cardiovascular Surgery, College of Medicine, Gyeongsang National University and Gyeongsang National University Hospital, Jinju 52727, Korea.
Dawon KangDepartment of Physiology and Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Korea.ORCID 0000-0001-7402-7298
Gyeongsang National University · KREwha Womans University Medical Center · KRGyeongsang National University Hospital · KR

Funding

Biomedical Research Institute Fund from the Gyeongsang National University Hospital GNUHBIF-2015-0009Ministry of Oceans and Fisheries PJT200671National Research Foundation of Korea NRF-2015R1A-5A-2008833National Research Foundation of Korea NRF-2018R1A2B6001446
6 · The paper itself

Abstract

Sea hare-derived compounds induce macrophage activation and reduce asthmatic parameters in mouse models of allergic asthma. These findings led us to study the role of sea hare hydrolysates (SHH) in cancer pathophysiology. SHH treatment-induced M1 macrophage activation in RAW264.7 cells, peritoneal macrophages, and THP-1 cells, as did lipopolysaccharide (LPS) (+ INF-γ), whereas SHH reduced interleukin (IL)-4 (+IL-13)-induced M2 macrophage polarization. In addition, SHH treatment inhibited the actions of M1 and M2 macrophages, which have anticancer and pro-cancer effects, respectively, in non-small cell lung cancer cells (A549 and HCC-366) and tumor-associated macrophages (TAMs). Furthermore, SHH induced G2/M phase arrest and cell death in A549 cells. SHH also downregulated STAT3 activation in macrophages and A549 cells, and the down-regulation was recovered by colivelin, a STAT3 activator. SHH-induced reduction of M2 polarization and tumor growth was blocked by colivelin treatment. SHH-induced cell death did not occur in the manner of apoptotic signaling pathways, while the death pattern was mediated through pyroptosis/necroptosis, which causes membrane rupture, formation of vacuoles and bleb, activation of caspase-1, and secretion of IL-1β in SHH-treated A549 cells. However, a combination of SHH and colivelin blocked caspase-1 activation. Z-YVAD-FMK and necrostatin-1, pyrotosis and necroptosis inhibitors, attenuated SHH's effect on the cell viability of A549 cells. Taken together, SHH showed anticancer effects through a cytotoxic effect on A549 cells and a regulatory effect on macrophages in A549 cells. In addition, the SHH-induced anticancer effects were mediated by non-apoptotic regulated cell death pathways under STAT3 inhibition. These results suggest that SHH may be offered as a potential remedy for cancer immunotherapy.

Indexed as

immune modulationlung cancermacrophage polarizationnecroptosispyroptosissea hare hydrolysates

Identifiers

PMID32204484
PMCPMC7140097
OpenAlexW3011233527

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.