Unveiling the Prognostic Significance of Long Non-Coding RNA (lncRNA) PCAT1 in Invasive Breast Carcinoma

被引:0
|
作者
Chakrabarty, Brototi [1 ]
Afrin, Kashifa [2 ]
Islam, Sumaiya [3 ]
Kundu, Neloy [2 ]
Siraj, Md Afjalus [4 ]
机构
[1] Univ Oklahoma Hlth Sci Ctr OUHSC, Coll Pharm, Dept Pharmaceut Sci, Oklahoma City, OK USA
[2] Khulna Univ, Life Sci Sch, Pharm Discipline, Khulna, Bangladesh
[3] Auburn Univ, Dept Chem Engn, Auburn, AL USA
[4] Univ Hawaii Hilo, Daniel K Inouye Coll Pharm, Dept Pharmaceut Sci, Hilo, HI 96720 USA
来源
EURASIAN JOURNAL OF MEDICINE AND ONCOLOGY | 2024年 / 8卷 / 02期
关键词
Prostate cancer-associated transcript 1; long non-coding RNA; invasive breast carcinoma; estrogen receptor; cancer susceptibility candidate; EXPRESSION PROMOTES PROLIFERATION; POOR-PROGNOSIS; GASTRIC-CANCER; CELL-GROWTH; BIOMARKER; METASTASIS; PROGRESSION; OSTEOSARCOMA; LANDSCAPE; EVOLUTION;
D O I
10.14744/ejmo.2024.27775
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Prostate cancer-associated transcript 1 (PCAT1) is a long non-coding RNA (lncRNA), composed of more than 200 nucleotides which expression controls the proliferation, migration, invasion, and metastasis of different cancers. In this current study, we have analyzed the possible role of PCAT1 as a prognostic biomarker for invasive breast cancer (IBC). Method: Online web genomic portal cBioportal, GEPIA, PhosphoSitePlus, IGV, GENEMENIA, Ensembl, and ENCORI were used for this analysis. Result: Our analysis demonstrated that PCAT1 expression was higher in BRCA-mutated BC patients cells compared to normal cells (fold change similar to 1.56). Over time, patients with greater PCAT1 expression had a significantly lower overall survival rate (p- 5.539e-5). Besides, there was significant alteration of PCAT1 in PR (p- 1.672e-6), HER2 (p- 3.920e-4) negative, and ER (p- 3.190e-6) positive primary IBC samples. In addition, a correlation was also found with the alteration of PCAT1 and the histologic grade of the IBC (p- >10-10). Moreover, the co-occurrence of PCAT1 with the oncogenes of CASC family, i.e., CASC8, CASC11, and CASC19 in IBC was identified. The PCAT1, CASC8, CASC11, and CASC19 have genomic location, named chr8q24, which contains the loci responsible for different cancers including BC. Conclusion: These findings indicate the possible association of PCAT1 expression with poor clinical outcomes and co-occurrence with previously established oncogenes as well as biomarkers suggests its usefulness as a prognostic biomarker in IBC.
引用
收藏
页码:173 / 184
页数:12
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