Evidence map›Paper›PMID 39847292›Full record

ArticleDoklady. Biochemistry and biophysics2025

Inhibition of Renal Cell Carcinoma Growth by 1,3-thiazin-6-one Through Targeting the Inflammatory Reaction.

Hongmei Zhou, Xin Li, Dongju Liu

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In one paragraph

Article in Doklady. Biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Hongmei ZhouNephrology Department, Zhongxian People's Hospital of Chongqing, Zhongxian County, 404300, Chongqing, China.
Xin LiNephrology Department, Zhongxian People's Hospital of Chongqing, Zhongxian County, 404300, Chongqing, China.
Dongju LiuNephrology Department, Liangping Hospital, Liangping District People's Hospital of Chongqing, 405299, Chongqing, China. ldj891013@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study examined the underlying mechanism and the effect of 1,3-thiazin-6-one on the growth of renal cancer. The findings showed that 1,3-thiazin-6-one treatment inhibited the growth of xenograft tumors in a dose-dependent manner in mice model of renal cancer. Furthermore, when 1,3-thiazin-6-one was administered in a dose-dependent manner to mice with renal cancer, the expression of the proteins p-PI3K and p-Akt significantly decreased. In mice model of renal cancer, 1,3-thiazin-6-one treatment also inhibited p-mTOR expression. In a model of renal cancer in mice, the 1,3-thiazin-6-one therapy specifically targeted the expression of nuclear factor κB (NF κB) and signal transducer and activator of transcription 3 (STAT3). Renal cancer cells' vitality was significantly (p < 0.05) reduced in a dose-dependent manner upon exposure to 1,3-thiazin-6-one. It also prevents invasiveness of the renal cancer cells in addition to suppression of colony forming potential. In summary, the 1,3-thiazin-6-one blocks the growth of kidney cancer by focusing on the pathways that trigger the inflammatory cascade. Therefore, 1,3-thiazin-6-one might be developed as a significant medicinal agent to cure renal cancer.

Indexed as

Antineoplastic AgentsCarcinoma, Renal CellInflammationKidney NeoplasmsThiazinesAnimalsCell Line, TumorCell ProliferationHumansMiceMice, Inbred BALB CMice, NudeNF-kappa BSTAT3 Transcription FactorXenograft Model Antitumor AssaysAntineoplastic AgentsNF-kappa BSTAT3 Transcription FactorThiazines1,3-thiazin-6-oneanticancerchemotherapydrug developmentinflammatory cascade

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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.