Evidence map›Paper›PMID 36185620›Full record

ArticleJournal of oncology2022

The Interaction of the IFN

Yaguang Han, Yan Zhang, Ying Tian, Miao Zhang, Cheng Xiang, Qiang Zhen, Jiabao Liu, Yanhong Shang, Yiyi Zhao, Huarui Si and 1 more

Abstract read
In one paragraph

Article in Journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. [Therapeutic mechanism of hederagenin, an active component inNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
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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

11 authors.

Yaguang HanDepartment of Oncology, Shijiazhuang People's Hospital, Shijiazhuang 050030, China.ORCID https://orcid.org/0000-0002-9023-9001
Yan ZhangDepartment of Oncology, Shijiazhuang People's Hospital, Shijiazhuang 050030, China.ORCID https://orcid.org/0000-0003-2211-8539
Ying TianHeBei Reproductive Hospital, Shijiazhuang 050000, China.
Miao ZhangDepartment of Oncology, Shijiazhuang People's Hospital, Shijiazhuang 050030, China.
Cheng XiangDepartment of Oncology, Shijiazhuang People's Hospital, Shijiazhuang 050030, China.
Qiang ZhenDepartment of Thoracic Surgery, Shijiazhuang People's Hospital, Shijiazhuang 050000, China.
Jiabao LiuDepartment of Thoracic Surgery, Shijiazhuang People's Hospital, Shijiazhuang 050000, China.
Yanhong ShangDepartment of Oncology, Affiliated Hospital of Hebei University, Baoding 071000, China.
Yiyi ZhaoDepartment of Oncology, Shijiazhuang People's Hospital, Shijiazhuang 050030, China.
Huarui SiDepartment of Oncology, Shijiazhuang People's Hospital, Shijiazhuang 050030, China.
Aixia SuiDepartment of Oncology, Hebei General Hospital, Shijiazhuang 050051, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: It was reported that the EGFR (epidermal growth factor receptor) mutation status was related to primary immune resistance in NSCLC (non-small-cell lung cancer). ICIs (immune checkpoint inhibitors) have poor efficacy and large side effects for people with EGFR mutation. EGFR mutation was considered as a sign of immune therapeutic resistance, but its underlying mechanism is difficult to be determined. Combined with our research basis, we tried to explore the possible mechanism of primary drug resistance in EFGR mutant lung adenocarcinoma through the interaction between the JAK/STAT1 and JAK/STAT3 pathway. Materials and Methods: Cell apoptosis and viability test were used to study the role of the JAK/STAT signalling pathway in lung adenocarcinoma cell survival. Western blot, RT-PCR, and flow cytometry were employed to explore the changes of expression in JAK1/2, STAT1/3, PD-L1, and related signal molecules in the case of activation or inhibition of the JAK/STAT3 signalling pathway. Results: With inhibition of inhibiting the JAK/STAT3 signalling pathway by STAT3 inhibitors, we found IFN Conclusions: The absence of the IFN

Identifiers

PMID36185620
PMCPMC9519310

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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.