Qixia Xu's research while affiliated with Chinese Academy of Sciences and other places
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Publications (22)
Senescent cells remain metabolically active, but their metabolic landscape and resulting implications remain underexplored. Here we highlight upregulation of pyruvate dehydrogenase kinase 4 (PDK4) upon cellular senescence, a tendency adversely correlated with cancer patient survival after chemotherapy. Senescent cells exhibit increased aerobic glyc...
The tumor microenvironment (TME) represents a milieu enabling cancer cells to develop malignant properties, while concerted interactions between cancer and stromal cells frequently shape an “activated/reprogramed” niche to accelerate pathological progression. Here we report that a soluble factor epiregulin (EREG) is produced by senescent stromal ce...
Cellular senescence is a state of stable growth arrest, usually accompanied by development of the senescence-associated secretory phenotype (SASP). Although senescent cells remain metabolically active, little is known about their metabolic landscape and in vivo pathophysiological implications. Here we show that expression of the pyruvate dehydrogen...
Cellular senescence is a state of stable growth arrest, usually accompanied by development of the senescence-associated secretory phenotype (SASP). Although senescent cells remain metabolically active, little is known about their metabolic landscape and in vivo pathophysiological implications. Here we show that expression of the pyruvate dehydrogen...
Ageing-associated functional decline of organs and increased risk for age-related chronic pathologies is driven in part by the accumulation of senescent cells, which develop the senescence-associated secretory phenotype (SASP). Here we show that procyanidin C1 (PCC1), a polyphenolic component of grape seed extract (GSE), increases the healthspan an...
Cellular senescence restrains the expansion of neoplastic cells through several layers of regulation. We report that the histone H3-specific demethylase KDM4 is expressed as human stromal cells undergo senescence. In clinical oncology, upregulated KDM4 and diminished H3K9/H3K36 methylation correlate with poorer survival of patients with prostate ca...
Aging causes functional decline of multiple organs and increases the risk of age-related pathologies. In advanced lives, accumulation of senescent cells, which develop the senescence-associated secretory phenotype (SASP), promotes chronic inflammation and causes diverse conditions. Here we report the frontline outcome of screening a natural product...
Aging causes functional decline of multiple organs and increases the risk of age-related pathologies. In advanced lives, accumulation of senescent cells, which develop the senescence-associated secretory phenotype (SASP), promotes chronic inflammation and causes diverse conditions. Here we report the frontline outcome of screening a natural product...
Cellular senescence restrains the expansion of neoplastic cells through several layers of regulation, including epigenetic decoration of chromatin structure and functional modulation of bioactive components. Here we report that expression of the histone H3-specific demethylase KDM4 is upregulated in human stromal cells upon cellular senescence. In...
Cellular senescence restrains the expansion of neoplastic cells through several layers of regulation, including epigenetic decoration of chromatin structure and functional modulation of bioactive components. Here we report that expression of the histone H3-specific demethylase KDM4 is upregulated in human stromal cells upon cellular senescence. In...
Cellular senescence is a potent tumor-suppressive program that prevents neoplastic events. Paradoxically, senescent cells develop an inflammatory secretome, termed the senescence-associated secretory phenotype, which is implicated in age-related pathologies including cancer. Here, we report that senescent cells actively synthesize and release small...
Liu Han Qila Long Shenjun Li- [...]
Yu Sun
Cellular senescence is a potent tumor-suppressive program that prevents neoplastic events. Paradoxically, senescent cells develop an inflammatory secretome, termed the senescence-associated secretory phenotype (SASP) and implicated in age-related pathologies including cancer. Here we report that senescent cells actively synthesize and release small...
Aging is characterized by a progressive loss of physiological integrity, while cancer represents one of the primary pathological factors that severely threaten human lifespan and healthspan. In clinical oncology, drug resistance limits the efficacy of most anticancer treatments, and identification of major mechanisms remains a key to solve this cha...
p>Therapeutic resistance is the major barrier to conquer human cancer, the most lethal pathology that claims numerous lives per year. Although identification of resistance mechanisms is the key to develop optimal strategies, progress has been limited due to long term failure to reveal the most critical targets. Cancer cells exhibit high plasticity...
Therapeutic resistance is the major barrier to conquer human cancer, the most lethal pathology that claims numerous lives per year. Although identification of resistance mechanisms is the key to develop optimal strategies, progress has been limited due to long term failure to reveal the most critical targets. Cancer cells exhibit high plasticity ev...
Fei Chen Qilai Long Da Fu- [...]
Yu Sun
Chemotherapy and radiation not only trigger cancer cell apoptosis but also damage stromal cells in the tumour microenvironment (TME), inducing a senescence-associated secretory phenotype (SASP) characterized by chronic secretion of diverse soluble factors. Here we report serine protease inhibitor Kazal type I (SPINK1), a SASP factor produced in hum...
Boyi Zhang Da Fu Qixia Xu- [...]
Yu Sun
The senescence-associated secretory phenotype (SASP) can be provoked by side effects of therapeutic agents, fueling advanced complications including cancer resistance. However, the intracellular signal network supporting initiation and development of the SASP driven by treatment-induced damage remains unclear. Here we report that the transcription...
Boyi Zhang Fei Chen Qixia Xu- [...]
Yu Sun
Development of ovarian cancer involves the co-evolution of neoplastic cells together with the adjacent microenvironment. Steps of malignant progression including primary tumor outgrowth, therapeutic resistance, and distant metastasis are not determined solely by genetic alterations in ovarian cancer cells, but considerably shaped by the fitness adv...
Although there is a large body of literature regarding amphiregulin (AREG) in human cancer, most knowledge focuses on its cell-autonomous functions in epithelial malignancies. Recent studies revealed that AREG is also present in the tumor microenvironment (TME) and contributes to therapeutic resistance. We discuss emerging concepts of AREG tumor bi...
Citations
... High expression of EREG was associated with tumor stage, metastasis and survival in human cancer patients. DNA-damaging agents (DDAs), such as bleomycin, mitoxantrone, and doxorubicin, induced the expression of EREG in stromal cells (115). Stromal EREG The role of E3 ubiquitin ligases and DUBs in regulation of PD-1/PD-L1 in cancer. ...
... Age-related diseases and their corresponding social burden are increasing. Ageassociated immune senescent modifications might lead to a decrease in the immune system, chronic inflammation, in addition to weakness, chronic disease, and loss of function among old people [247]. Translating approaches that target senescent cells into clinical practice could have a major impact on curing a range of diseases that occur with age and perhaps change our perspective of ageing. ...
... Notably, some Jumonji KDMs were increased in response to CP treatment ( Fig S1A). This is consistent with previous studies showing expression of different Jumonji KDMs induced in response to CP. 16,17 CPR cells expressed elevated levels of multiple Jumonji KDMs compared to parental controls, both basally and in response to CP. Some of these KDMs (KDM3A, KDM4B, KDM5A, and KDM6A) were commonly overexpressed in all 3 CPR cell populations (names in red in Fig. S1A). ...
... There are many V. vinifera cultivars and the cold hardiness of different varieties varies, with few V. vinifera varieties are suitable for cultivation in any specific country or region (Zhan and Li, 2010;Wang et al., 2021b). Most research on V. vinifera has focused on cultivation management (Ju et al., 2019;Yue et al., 2020;Wang et al., 2021a;Yue et al., 2021), fruit quality regulation (Bohan et al., 2020;Yang N. et al., 2021), wine-making characteristics Wei et al., 2022), grape and wine nutrition (Cheng et al., 2021;Xu et al., 2021;Yang C. et al., 2021), and hardiness improvement Wan et al., 2021;Wang et al., 2021c;Wang et al., 2022), but there has been little comprehensive work to determine the most appropriate methods for the evaluation of cold hardiness in V. vinifera. Most methods used thus far to investigate cold hardiness are relatively simple methods that are not targeted, so the results obtained using different cold hardiness evaluation methods will be different (He, 2015). ...
... At the transcriptional level, several transcription factors (NF-κB, C/EBP-β) and upstream regulators (p38 MAPK, GATA4, p53, and ATM) have been described to either positively or negatively regulate SASP gene expression [16,[19][20][21][22][23][24][25]. The SASP is also regulated at both the epigenetic [26][27][28][29][30][31][32] and translational level [17,33]. Recent publications suggest that the initiation of AGING SASP gene transcription during OIS is likely due to loss of lamin B1 (LMNB1) and nuclear integrity [34,35], leading to the accumulation of cytoplasmic chromatin fragments (CCFs) [36,37]. ...
... Recent work along with our transcriptome profiles showed that TGF-β signaling is dysregulated in senescent MSCs [16,17]. Studies have also demonstrated that senescent cell-secreted vesicles can enhance aggressive phenotypes during cell-cell interaction via TGF-β signaling pathways [18][19][20]. Therefore, we further examined significantly altered genes for each of the related transcriptome pathways ( Figure 1C-1F). ...
... However, their role in the development of tumours has also been shown [75]. Recent studies revealed that amphiregulin is produced by senescent cells and its presence is a negative background provoking expression of programmed cell death 1 ligand (PD-L1) and cancer development [76,77], (Figure 2). This role of T regs associated with age-dependent carcinogenesis is being actively investigated. ...
... The size distribution was analyzed using a 2200 TapeStation Instrument (Agilent Technologies). Based on DNA concentration and average fragment size, libraries were pooled and denatured as previously described [71]. The libraries were sequenced on a HiSeq 2500 system using 100-bp paired-end sequencing (Illumina) to generate approximately 50-80 million reads per sample. ...
... Depletion of ZSCAN4 was found to have inhibitory effect on tumor growth in HNSCC [30]. Moreover, Zhang et al. found that ZSCAN4 expression is increased in DNA-damaged stromal cells that leads to a senescence-associated secretory phenotype (SASP), mediated by the ATM/TRAF6/TAK1/p65 signaling axis [31]. They also disclosed that targeting TAK1 in vivo increases chemosensitization and promotes tumor regression. ...
... EpCAM has been detected in exosomes isolated from serum of patients with ovarian cancer, which confirmed the presence of diagnostic miRNAs in exosomes (50). A further study showed that serum exosomes from patients with ovarian cancer contained higher levels of mRNA and miRNA than those from healthy people (51), which provided a basis for tumor-derived exosomes to participate in the transport of genetic material between cells. This also demonstrates that diagnostic miRNAs in serum exosomes of patients with ovarian cancer can be used for the diagnosis of ovarian cancer (52,53). ...