ArticleAsian Pacific journal of cancer prevention : APJCP2026
Prognostic Significance of miR-145, NANOG, OCT4, and KLF4 in Triple-Negative Breast Cancer.
Article in Asian Pacific journal of cancer prevention : APJCP, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAmong women, breast cancer is the leading cause of cancer-related deaths. OCT4, NANOG, and KLF4 are markers of cancer stem cells. miR-145 is a tumor suppressor in many cancers. We aimed to estimate the expression of miR-145 and cancer stem cell markers in triple-negative breast cancer (TNBC) and to investigate their correlations with clinicopathological characteristics and outcomes in these patients.
methodsThe study included 90 female patients with TNBC. Grade III represented 64.4% of cases, while Grades I and II represented 11.1% and 24.4%, respectively. Seventy-two patients (80%) had lymph node involvement. Breast tissues from malignant and adjacent control tissues were used for RNA extraction and subsequent analysis of miR-145 expression. Histopathological and immunohistochemical analyses were also performed.
resultsIt was found that lymph node (LN)-positive tumors exhibited higher OCT4 levels compared to LN-negative tumors (P = 0.039). Additionally, tumors with extensive intraductal invasion and relapse showed lower KLF4 levels (P = 0.02 and <0.001, respectively). Downregulated miR-145 expression was associated with higher stages, relapse, and mortality (P < 0.001 for each), LN involvement (P = 0.002), and capsular invasion (P = 0.02). There were significant strong positive correlations between miR-145 and DFS (r = 0.920, P < 0.001) and OS (r = 0.813, P < 0.001). However, significant weak negative correlations were found with KLF4 (r = -0.242, P = 0.022), NANOG (r = -0.305, P = 0.009), OCT4 (r = -0.255, P = 0.014), tumor size (r = -0.247, P = 0.019), and the number of positive LNs (r = -0.481, P < 0.001). OCT4 levels showed significant positive correlations with NANOG (r = 0.328, P = 0.002) and KLF4 expression (r = 0.344, P = 0.001). Moreover, a significant positive correlation was detected between KLF4 levels and DFS (r = 0.255, P = 0.015). The log-rank test showed a significant association of KLF4 with DFS (P = 0.005).
conclusionmiR-145 and KLF4 are possible prognostic markers in TNBC. This was reflected by the positive correlations between miR-145 and both DFS and OS, and between KLF4 levels and DFS.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.