TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer

ObjectiveOvarian cancer (OV) is the most fatal and frequent type of gynecological malignancy worldwide. TIMELESS (TIM), as a circadian clock gene, has been found to be highly expressed and predictive of poor prognosis in various cancers. However, the function of TIM in OV is not known. This study wa...

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Main Authors: Xin Xing, Fei Gu, Lanyu Hua, Xiaoxiao Cui, Dongxue Li, Zhiyong Wu, Rong Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.732058/full
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author Xin Xing
Fei Gu
Lanyu Hua
Xiaoxiao Cui
Dongxue Li
Zhiyong Wu
Rong Zhang
Rong Zhang
author_facet Xin Xing
Fei Gu
Lanyu Hua
Xiaoxiao Cui
Dongxue Li
Zhiyong Wu
Rong Zhang
Rong Zhang
author_sort Xin Xing
collection DOAJ
description ObjectiveOvarian cancer (OV) is the most fatal and frequent type of gynecological malignancy worldwide. TIMELESS (TIM), as a circadian clock gene, has been found to be highly expressed and predictive of poor prognosis in various cancers. However, the function of TIM in OV is not known. This study was designed to investigate the biological functions and underlying mechanisms of TIM during OV progression.MethodsCell viability assay, cell migration assay, immunohistochemistry staining, qPCR analyses, and tumor xenograft model were used to identify the functions of TIM in OV. Bioinformatics analyses, including GEPIA, cBioPortal, GeneMANIA, and TIMER, were used to analyze the gene expression, genetic alteration, and immune cell infiltration of TIM in OV.ResultsTIM is highly expressed in OV patients. TIM knockdown inhibited OV cell proliferation, migration, and invasion both in vitro and in vivo. Genetic alteration of TIM was identified in patients with OV. TIM co-expression network indicates that TIM had a wide effect on the immune cell infiltration and activation in OV. Further analysis and experimental verification revealed that TIM was positively correlated with macrophages infiltration in OV.ConclusionsOur study unveiled a novel function of highly expressed TIM associated with immune cell especially macrophages infiltration in OV. TIM may serve as a potential prognostic biomarker and immunotherapy target for OV patients.
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spelling doaj.art-a864324e6b7f4f90997a8224ff75fb182022-12-21T18:28:43ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-08-011110.3389/fonc.2021.732058732058TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian CancerXin Xing0Fei Gu1Lanyu Hua2Xiaoxiao Cui3Dongxue Li4Zhiyong Wu5Rong Zhang6Rong Zhang7Department of Obstetrics and Gynecology, Fengxian Hospital Affiliated to the Southern Medical University, Shanghai, ChinaDepartment of Obstetrics and Gynecology, Fengxian Hospital Affiliated to the Southern Medical University, Shanghai, ChinaThe Third School of Clinical Medicine, Southern Medical University, Guangzhou, ChinaDepartment of Obstetrics and Gynecology, Fengxian Hospital Affiliated to the Southern Medical University, Shanghai, ChinaShanghai Cancer Institute, Shanghai, ChinaGynecology Department, Shanghai Obstetrics and Gynecology Hospital of Fudan University, Shanghai, ChinaDepartment of Obstetrics and Gynecology, Fengxian Hospital Affiliated to the Southern Medical University, Shanghai, ChinaThe Third School of Clinical Medicine, Southern Medical University, Guangzhou, ChinaObjectiveOvarian cancer (OV) is the most fatal and frequent type of gynecological malignancy worldwide. TIMELESS (TIM), as a circadian clock gene, has been found to be highly expressed and predictive of poor prognosis in various cancers. However, the function of TIM in OV is not known. This study was designed to investigate the biological functions and underlying mechanisms of TIM during OV progression.MethodsCell viability assay, cell migration assay, immunohistochemistry staining, qPCR analyses, and tumor xenograft model were used to identify the functions of TIM in OV. Bioinformatics analyses, including GEPIA, cBioPortal, GeneMANIA, and TIMER, were used to analyze the gene expression, genetic alteration, and immune cell infiltration of TIM in OV.ResultsTIM is highly expressed in OV patients. TIM knockdown inhibited OV cell proliferation, migration, and invasion both in vitro and in vivo. Genetic alteration of TIM was identified in patients with OV. TIM co-expression network indicates that TIM had a wide effect on the immune cell infiltration and activation in OV. Further analysis and experimental verification revealed that TIM was positively correlated with macrophages infiltration in OV.ConclusionsOur study unveiled a novel function of highly expressed TIM associated with immune cell especially macrophages infiltration in OV. TIM may serve as a potential prognostic biomarker and immunotherapy target for OV patients.https://www.frontiersin.org/articles/10.3389/fonc.2021.732058/fullovarian cancermacrophageschemokinesbioinformatic analysisTIM
spellingShingle Xin Xing
Fei Gu
Lanyu Hua
Xiaoxiao Cui
Dongxue Li
Zhiyong Wu
Rong Zhang
Rong Zhang
TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer
Frontiers in Oncology
ovarian cancer
macrophages
chemokines
bioinformatic analysis
TIM
title TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer
title_full TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer
title_fullStr TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer
title_full_unstemmed TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer
title_short TIMELESS Promotes Tumor Progression by Enhancing Macrophages Recruitment in Ovarian Cancer
title_sort timeless promotes tumor progression by enhancing macrophages recruitment in ovarian cancer
topic ovarian cancer
macrophages
chemokines
bioinformatic analysis
TIM
url https://www.frontiersin.org/articles/10.3389/fonc.2021.732058/full
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