Identification of Differentiation-Related Biomarkers in Liposarcoma Tissues Using Weighted Gene Co-Expression Network Analysis

被引:0
作者
Zhao, Huanhuan [1 ]
Zhang, Guochuan [1 ]
机构
[1] Hebei Med Univ, Hosp 3, Dept Orthoped Oncol, Shijiazhuang 050051, Hebei, Peoples R China
关键词
WGCNA; LASSO analysis; liposarcoma; differentiation-related biomarker; differential diagnosis; CANCER;
D O I
10.23812/j.biol.regul.homeost.agents.20233712.644
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: A thorough diagnosis of liposarcoma is essential to develop an optimal therapy. This study aimed to identify differentiation-related biomarkers in liposarcoma. Methods: Expression profiling data were downloaded from the Gene Expression Omnibus (GEO) database. Modules correlated with dedifferentiated liposarcoma were identified using weighted gene co-expression network analysis (WGCNA). Differentiallyexpressed genes were identified utilizing the limma R package. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were conducted with the clusterProfiler R package. Hub genes were identified by least absolute shrinkage and selection operator (LASSO) analysis. Survival analysis was performed using survival and survminer R packages. Results: The brown module was the most positively correlated module with dedifferentiated liposarcoma, while the turquoise module exhibited the strongest negative correlation with dedifferentiated liposarcoma. Forty-nine upregulated common genes were found by intersecting the upregulated differentially-expressed genes with the co-expressed genes in the brown module, and 177 downregulated common genes were found by intersecting the downregulated differentially-expressed genes with the coexpressed genes in the turquoise module. GO and KEGG analyses revealed that upregulated common genes were abundant in cell division and tumor-related pathways, while downregulated common genes were involved in cellular metabolism and metabolismrelated pathways. ADIPOQ, i7BE2C, and PRC1 were screened out as biomarkers which might distinguish dedifferentiated and well-differentiated liposarcoma. Dedifferentiated liposarcoma patients with low ADIPOQ levels displayed a significantly shorter distant recurrence-free survival than those with high ADIPOQ levels. Conclusion: ADIPOQ, i7BE2C, and PRC1 are potential differentiation-related biomarkers in liposarcoma tissues. ADIPOQ has the potential to be a novel prognostic biomarker for patients with dedifferentiated liposarcoma.
引用
收藏
页码:6807 / 6819
页数:13
相关论文
共 30 条
[1]   Cell cycle regulation and anticancer drug discovery [J].
Bai, Jingwen ;
Li, Yaochen ;
Zhang, Guojun .
CANCER BIOLOGY & MEDICINE, 2017, 14 (04) :348-362
[2]   SAR405838: A Novel and Potent Inhibitor of the MDM2:p53 Axis for the Treatment of Dedifferentiated Liposarcoma [J].
Bill, Kate Lynn J. ;
Garnett, Jeannine ;
Meaux, Isabelle ;
Ma, XiaoYen ;
Creighton, Chad J. ;
Bolshakov, Svetlana ;
Barriere, Cedric ;
Debussche, Laurent ;
Lazar, Alexander J. ;
Prudner, Bethany C. ;
Casadei, Lucia ;
Braggio, Danielle ;
Lopez, Gonzalo ;
Zewdu, Abbie ;
Bid, Hemant ;
Lev, Dina ;
Pollock, Raphael E. .
CLINICAL CANCER RESEARCH, 2016, 22 (05) :1150-1160
[3]   Beyond targeting amplified MDM2 and CDK4 in well differentiated and dedifferentiated liposarcomas: From promise and clinical applications towards identification of progression drivers [J].
Cassinelli, Giuliana ;
Pasquali, Sandro ;
Lanzi, Cinzia .
FRONTIERS IN ONCOLOGY, 2022, 12
[4]   ADIPOQ/adiponectin induces cytotoxic autophagy in breast cancer cells through STK11/LKB1-mediated activation of the AMPK-ULK1 axis [J].
Chung, Seung J. ;
Nagaraju, Ganji Purnachandra ;
Nagalingam, Arumugam ;
Muniraj, Nethaji ;
Kuppusamy, Panjamurthy ;
Walker, Alyssa ;
Woo, Juhyung ;
Gyorffy, Balazs ;
Gabrielson, Ed ;
Saxena, Neeraj K. ;
Sharma, Dipali .
AUTOPHAGY, 2017, 13 (08) :1386-1403
[5]   Genetic variation in the ADIPOQ gene and serum adiponectin increase the risk of bladder cancer [J].
Elsalem, Lina ;
Alfaqih, Mahmoud A. ;
Al Bashir, Samir ;
Halalsheh, Omar ;
Basheer, Haneen A. ;
Mhedat, Khawla ;
Khader, Yousef ;
Pors, Klaus .
JOURNAL OF APPLIED BIOMEDICINE, 2022, 20 (03) :106-113
[6]   The AMPK pathway in fatty liver disease [J].
Fang, Chunqiu ;
Pan, Jianheng ;
Qu, Ning ;
Lei, Yuting ;
Han, Jiajun ;
Zhang, Jingzhou ;
Han, Dong .
FRONTIERS IN PHYSIOLOGY, 2022, 13
[7]   Combination of PPARγ Agonist Pioglitazone and Trabectedin Induce Adipocyte Differentiation to Overcome Trabectedin Resistance in Myxoid Liposarcomas [J].
Frapolli, Roberta ;
Bello, Ezia ;
Ponzo, Marianna ;
Craparotta, Ilaria ;
Mannarino, Laura ;
Ballabio, Sara ;
Marchini, Sergio ;
Carrassa, Laura ;
Ubezio, Paolo ;
Porcu, Luca ;
Brich, Silvia ;
Sanfilippo, Roberta ;
Casali, Paolo Giovanni ;
Gronchi, Alessandro ;
Pilotti, Silvana ;
D'Incalci, Maurizio .
CLINICAL CANCER RESEARCH, 2019, 25 (24) :7565-7575
[8]   Regularization Paths for Generalized Linear Models via Coordinate Descent [J].
Friedman, Jerome ;
Hastie, Trevor ;
Tibshirani, Rob .
JOURNAL OF STATISTICAL SOFTWARE, 2010, 33 (01) :1-22
[9]   Expression Profiling of Liposarcoma Yields a Multigene Predictor of Patient Outcome and Identifies Genes That Contribute to Liposarcomagenesis [J].
Gobble, Ryan M. ;
Qin, Li-Xuan ;
Brill, Elliott R. ;
Angeles, Christina V. ;
Ugras, Stacy ;
O'Connor, Rachael B. ;
Moraco, Nicole H. ;
DeCarolis, Penelope L. ;
Antonescu, Cristina ;
Singer, Samuel .
CANCER RESEARCH, 2011, 71 (07) :2697-2705
[10]  
Hernandez-Ortega Sara, 2019, Exp Mol Med, V51, P1