scholarly journals miR-589 promotes gastric cancer aggressiveness by a LIFR-PI3K/AKT-c-Jun regulatory feedback loop

Author(s):  
Feifei Zhang ◽  
Kaitao Li ◽  
Mingxin Pan ◽  
Weidong Li ◽  
Juan Wu ◽  
...  
2015 ◽  
Vol 58 ◽  
pp. 83-100 ◽  
Author(s):  
Selena Gimenez-Ibanez ◽  
Marta Boter ◽  
Roberto Solano

Jasmonates (JAs) are essential signalling molecules that co-ordinate the plant response to biotic and abiotic challenges, as well as co-ordinating several developmental processes. Huge progress has been made over the last decade in understanding the components and mechanisms that govern JA perception and signalling. The bioactive form of the hormone, (+)-7-iso-jasmonyl-l-isoleucine (JA-Ile), is perceived by the COI1–JAZ co-receptor complex. JASMONATE ZIM DOMAIN (JAZ) proteins also act as direct repressors of transcriptional activators such as MYC2. In the emerging picture of JA-Ile perception and signalling, COI1 operates as an E3 ubiquitin ligase that upon binding of JA-Ile targets JAZ repressors for degradation by the 26S proteasome, thereby derepressing transcription factors such as MYC2, which in turn activate JA-Ile-dependent transcriptional reprogramming. It is noteworthy that MYCs and different spliced variants of the JAZ proteins are involved in a negative regulatory feedback loop, which suggests a model that rapidly turns the transcriptional JA-Ile responses on and off and thereby avoids a detrimental overactivation of the pathway. This chapter highlights the most recent advances in our understanding of JA-Ile signalling, focusing on the latest repertoire of new targets of JAZ proteins to control different sets of JA-Ile-mediated responses, novel mechanisms of negative regulation of JA-Ile signalling, and hormonal cross-talk at the molecular level that ultimately determines plant adaptability and survival.


Aging ◽  
2020 ◽  
Author(s):  
Yu-En Tan ◽  
Yao Xing ◽  
Ban-Lai Ran ◽  
Chao Zhang ◽  
Si-Wei Pan ◽  
...  

2020 ◽  
Author(s):  
Yung-Yu Hsieh ◽  
Shui-Yi Tung ◽  
Hung-Yu Pan ◽  
Te-Sheng Chang ◽  
Kuo-Liang Wei ◽  
...  

Abstract Background Fusobacterium nucleatum was previously found to become a dominant species in the gastric cancer-associated microbiota of patients from Taiwan. However, the prevalence of Fusobacterium nucleatum infection in gastric cancer has not been examined in a larger patient cohort. In addition, whether Fusobacterium nucleatum elicits a cellular response in gastric cancer remains unknown.Methods A study cohort of resected gastric cancer tissue specimens was examined using nested PCR to detect Fusobacterium nucleatum. In vitro coculture of Fusobacterium nucleatum was carried out to identify the alteration in the expression profile of patient-derived gastric cancer cell line.Results approximately one-third of gastric cancer tissues are positive for Fusobacterium nucleatum. Statistical analysis showed that the risk for Fusobacterium nucleatum infection is increased in late-stage cancer tissue specimens and incurs poorer survival in Helicobacter pylori-positive patients. In vitro coculture experiment shows a drastic interferon response activated only by a high multiplicity of infection, and the response peaks within 24 hours and subsides after 72 hours of incubation. Another set of response genes is the continuous increase of actins and their regulators with prolonged time of incubation, activated by both low and high multiplicity of infection.Conclusions Our data indicates that Fusobacterium nucleatum incites an inflammatory response from the cancer cells and promotes cell mobility, likely


2019 ◽  
Vol Volume 12 ◽  
pp. 7949-7962 ◽  
Author(s):  
Cao Zhang ◽  
Haiquan Qian ◽  
Ke Liu ◽  
Wei Zhao ◽  
Lei Wang

2020 ◽  
Vol 14 (10) ◽  
pp. 2629-2645
Author(s):  
Bei‐bei Lv ◽  
Ran‐ran Ma ◽  
Xu Chen ◽  
Guo‐hao Zhang ◽  
Lin Song ◽  
...  

2001 ◽  
Vol 183 (20) ◽  
pp. 5974-5981 ◽  
Author(s):  
Natividad Ruiz ◽  
Celeste N. Peterson ◽  
Thomas J. Silhavy

ABSTRACT The stationary-phase response exhibited by Escherichia coli upon nutrient starvation is mainly induced by a decrease of the ClpXP-dependent degradation of the alternate primary ς factor RpoS. Although it is known that the specific regulation of this proteolysis is exercised by the orphan response regulator SprE, it remains unclear how SprE's activity is regulated in vivo. Previous studies have demonstrated that the cellular content of SprE itself is paradoxically increased in stationary-phase cells in an RpoS-dependent fashion. We show here that this RpoS-dependent upregulation of SprE levels is due to increased transcription. Furthermore, we demonstrate that sprE is part of the two-generssA-sprE operon, but it can also be transcribed from an additional RpoS-dependent promoter located in therssA-sprE intergenic region. In addition, by using an in-frame deletion in rssA we found that RssA does not regulate either SprE or RpoS under the conditions tested.


Theranostics ◽  
2019 ◽  
Vol 9 (25) ◽  
pp. 7628-7647 ◽  
Author(s):  
Chao Wang ◽  
Min Shi ◽  
Jun Ji ◽  
Qu Cai ◽  
Jinling Jiang ◽  
...  

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