Many articles focus on the mysterious connection between microRNA and cancer!

In this article, the editor compiled a number of important research results recently published by scientists, focusing on the mysterious connection between microRNA and cancer! Share with everyone!

Image source: Correspondence to-Carol S.

[1] bioon.

In addition, the researchers also found that miR-708 can reduce the proliferation, survival and migration of lung cancer cells, which is partly due to the inhibitory effect of miR-708 on PGE2 signaling; in the article, the researchers also predicted a new miR-708 target As well as the regulators that regulate the expression of miR-708 in lung cancer, relevant research results indicate that the imbalance of miR-708 expression may promote the accelerated production of PGE2, which will enhance the production of tumor phenotypes of lung cancer cell clusters.

[2] bioon.

The researchers said that the rate of methylation of microRNAs can effectively distinguish cancer patients from healthy individuals; microRNAs can show abnormal expression in cancer tissues, and they are also relatively stable in body fluids, so they can be used as an indicator of cancer.

[3] bioon.

Initially, the researcher Paul B.

[4] bioon.

In order to reveal the relationship between miR-223 and inflammation, a Purdue University research team created a zebrafish completely missing miR-223, and then they removed a small piece of its fin.
"Inflammation is really strong," said Qing Deng, a professor of biological sciences at Purdue University and the corresponding author of the study.
"Neutrophils gather near the wound, and new cells are constantly coming over.
This is similar to the results in the literature, but we want to know why this is the case.
" A large number of gene expression analysis led them to the NF-kB pathway, NF- kB is a protein complex that regulates inflammation and cell proliferation that exists in almost all animal cells.
The increased activation level of this pathway is responsible for the increased level of inflammation, although inflammation is limited to the deep layer of epithelial tissue (basal layer).
This means that any therapeutic drug needs to reach the basal layer to be effective.

[5] bioon.
com/article/6712183.
html">Nat Commun: microRNA regulates tumor cell mobility

doi: 10.
1038/s41467-017-01197-w

Cancer cells can undergo cellular processes similar to embryonic development, allowing them to leave the original site, pass through the surrounding tissues, and form worsening tumors in peripheral organs.
In the latest issue of Nature Communications, researchers from the University of Basel discovered the molecular mechanisms that regulate this process.
In the process of embryonic development, epithelial cells can break through the restriction of cell aggregation, undergo specific differentiation, and then migrate to specific parts to form corresponding structures.
This process is called EMT (epithelial–mesenchymal transition).
The process is reversible, so there is also a way of MET.
This event recurs during embryonic development, which ultimately leads to the development of tissues and the human body.

Although it is very common during embryonic development, this process also occurs during the formation and deterioration of tumor cells.
Therefore, researchers are very interested in this feature of tumors.
Tumor cells can differentiate into EMT and MET, further gain stem cell activity, and develop resistance to cancer treatment.
EMT makes it easier for tumor cells to leave the original tissue, penetrate the surrounding packages, enter blood vessels and spread in the body, eventually leading to the death of the patient.

Image source: style="TEXT-JUSTIFY: inter-ideograph; TEXT-ALIGN: justify">[6] bioon.
com/article/6750894.
html">Nat Commun: miRNA drives cancer

doi: 10.
1038/s41467-020-14713-2

For a long time, researchers have believed that only one strand of double-stranded microRNA can silence genes.
Recently, a new study from Thomas Jefferson University showed that in certain cancer types, the two chains of certain microRNAs work together to promote the invasiveness and growth of cancer cells, which are two signs of poor prognosis for cancer patients.
The researchers said that the coordination of such activities is indeed surprising.
"Cancer Center (SKCC)-Jefferson Health.
We know that the two strands of miRNA will not target a uniform sequence, but despite this, we still see them working together.
"

This work was published in the journal Nature Communications.
The researchers obtained data from 5,200 cancer patient samples from 14 types of cancer and found that 26 types of microRNA pairs showed increased or decreased activity/abundance in a variety of cancers.

[7] bioon.
com/article/6723751.
html">Cell Death & Disease: lncRNA combined with miRNA promotes colon cancer proliferation and metastasis

doi: 10.
1038/s41419-018-0759-7

More and more evidences show that long non-coding RNA plays an important role in cancer progression, but there are still few studies on lncRNA SNHG7 in colorectal cancer, and how this molecule participates in colorectal cancer progression is still unclear.
Researchers from Dalian Medical University have studied the role of lncRNA SNHG7 in colorectal cancer, and the relevant research results have been published in the international academic journal Cell Death & Disease.

In this study, the researchers found that the expression of SNHG7 was significantly up-regulated in colorectal cancer tissues, especially in some more malignant cases.
Consistent with it, the expression level of SNHG7 in colorectal cancer cell lines is also significantly higher than that of normal colon cells.
The research results further show that overexpression of SNHG7 can promote the proliferation, migration and invasion of colorectal cancer cells, while the invasion and survival ability of cancer cells is significantly inhibited in the absence of SNHG7.

[8] bioon.
com/article/6685116.
html">Cell Death Dis: miRNA regulates the sensitivity of breast cancer chemotherapy

doi: 10.
1038/cddis.
2016.
194

Although the early diagnosis of breast cancer has made great progress, breast cancer is still the most important cancer affecting women's health in the world.
Neoadjuvant chemotherapy (NAC) is currently a key factor affecting the success rate of surgery.
In addition, NAC can also affect the sensitivity of tumor cells to chemotherapy.

Under normal circumstances, only a small number of breast cancer patients respond to NAC.
Unfortunately, there is no effective method to accurately predict the response patient population.
In addition, there is an urgent need to solve the serious negative effects of excessive chemotherapy on patients.
Some studies have tried to find biomarkers that can predict the responsiveness of NAC, thereby reducing the side effects and the risk of death caused by chemotherapy, which is of great significance for the treatment of breast cancer.
miRNAs are a class of highly conserved short non-coding RNAs that can negatively regulate gene expression.
Previous studies have found that a large number of miRNAs have increased or decreased expression in breast cancer cells, which further affects the occurrence of cancer cells and drug resistance.

[9] bioon.
com/article/6685913.
html">J Immunol: miRNA improves the efficiency of tumor immunotherapy

doi: 10.
4049/jimmunol.
1600182

miRNA is a type of short non-coding RNA, which is involved in the process of gene translation inhibition and mRNA degradation.
Previous studies have found that miRNA plays an important role in metabolism, cell proliferation, differentiation, apoptosis and development.
MiRNA dysregulation can trigger a variety of abnormal reactions in the body, including cancer, cardiovascular disease, neurodevelopmental disease, and liver disease.
In particular, studies have shown that miR-148/152 can inhibit TLR signal transmission in DC by regulating the activity of calmodulin-dependent protein kinase IIa.
In addition, DNA methylation plays an equally important role in the development and function of DC.

In order to study the role of miRNA in regulating DC response to TLR signals, Yifan Ma's research group from Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences conducted in-depth research, and the relevant results were published in the latest issue of Journal of Immunology.
First, the author compared the expression of various immune factors in common DC and tumor-related DC.
The results showed that the expression levels of CD86, MHCII, B7-H1 and other proteins in tumor-related DCs all decreased significantly.
In contrast, the expression levels of miR148a, miR148b, and miR152 in tumor-associated DCs were significantly higher than those of conventional DCs.

[10] bioon.
com/article/6730239.
html">Oncogene: Shanghai University scholars discovered microRNAs that promote lung cancer and revealed the mechanism of action

doi: 10.
1038/s41388-018-0534-3

Lung cancer is one of the most common malignant diseases in the world, including non-small cell lung cancer (about 85%) and small cell lung cancer (about 15%).
MicroRNA is a type of single-stranded non-coding RNA expressed in cells.
Previous studies have found that microRNA plays an important role in the development of lung cancer.
Recently, researchers from Shanghai University of Science and Technology reported in the international academic journal Oncogene that miR-411-5p/3p has a significant increase in expression in human non-small cell lung cancer tissues and cell lines.
Studies have shown that overexpression of miR-411-5p/3p can accelerate the proliferation and migration of non-small cell lung cancer cells, and can inhibit cell apoptosis.

In terms of mechanism, the researchers confirmed that SPRY4 is the direct target of miR-411-5p/3p, miR-411-5p/3p can promote lung tumor growth in vivo, significantly inhibit the expression of SPRY4, and induce the activation of EGFR and AKT signals.
It also induces the process of epithelial-mesenchymal transition in tumor tissues.
()

More exciting inventory! Stay tuned!