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This article is the original of Translational Medicine Network, please indicate the source for reprinting
Author: Mia
There is growing evidence that dysregulation of Myo1b (myosin 1b) expression has been extensively studied
in the development and progression of several tumors.
Recently, a research team has elucidated for the first time the role of Myo1b in autophagy regulation and angiogenesis in colon cancer cells, and revealed that it may be a viable predictive biomarker and therapeutic target
.
Recently, Yihong Chen, Nanzhu Xu, Chang Hong of Southern Medical University as the first authors, and Professor Jueyu Zhou as the corresponding author, published a report entitled "Myo1b promotes tumor progression and angiogenesis by inhibiting autophagic degradation of HIF-1α in colorectal" in Cell Death & Disease cancer"
.
This study found the potential function of Myo1b in colorectal cancer, and confirmed that Myo1b promotes colorectal cancer progression and angiogenesis by inhibiting the autophagy degradation of HIF-1α, suggesting that Myo1b has the role of
tumor promoting factor in colorectal cancer.
https://doi.
org/10.
1038/s41419-022-05397-1
Research background
01
Colorectal cancer (CRC) is the third most common cancer and second leading cause of cancer-related death worldwide, and its incidence is rising
rapidly among young and middle-aged adults.
Despite the availability of standard treatments including surgery, radiotherapy, and chemotherapy, there is currently no effective and reliable means to improve the survival rate
of patients with advanced colorectal cancer.
In addition, tumor-induced angiogenesis is a key marker of tumorigenesis and the cause of cancer cell growth and metastasis in CRC, so targeted antiangiogenic therapy is a promising option
for CRC therapy.
In recent years, there is new evidence that myosin is an important regulator of tumorigenesis and plays a role
in causing or suppressing tumors.
Myo1b is an important member of class I myosin and is involved in many key physiological and pathological processes
.
Abnormal expression of Myo1b has been detected in a variety of cancers, including prostate cancer, head and neck squamous cell carcinoma (HNSCC), cervical cancer, esophageal cancer (ESCC), and glioma, but research on the role of Myo1b in CRC tumorigenesis is still limited and its mechanism of action is unclear
.
Molecular mechanisms by which Myo1b promotes angiogenesis
02
In this study, Chen et al.
reported that Myo1b is highly expressed in colon cancer and is associated with
poorer survival.
High expression of Myo1b promotes proliferation, migration and invasion of CRC cells, while silencing Myo1b can inhibit tumor progression
in vitro and in vivo.
Further studies showed that Myo1b inhibited autophagosome-lysosomal fusion of CRC cells, enhanced VEGF secretion, and promoted angiogenesis
.
In terms of mechanism, Myo1b inhibits the autophagic degradation of HIF-1α, which in turn leads to the accumulation of HIF-1α, thereby enhancing VEGF secretion and ultimately promoting colorectal cancer tumor angiogenesis
.
Schematic diagram of Myo1b-mediated autophagy and angiogenesis mechanisms in colorectal cancer
Hypoxia-inducible factor-1α (HIF-1α) and vascular endothelial growth factor (VEGF) are two key regulators of angiogenesis
.
Previous studies have confirmed that some genes play a crucial role in tumor angiogenesis by acting directly on VEGF or stimulating angiogenesis
through the HIF-1α/VEGF pathway.
The HIF-1α/VEGF axis is an important component of
angiogenesis in various malignancies.
The results highlight the importance of the HIF-1α/VEGF pathway in Myo1b-mediated angiogenesis of
CRC cells.
Resources:
https://doi.
org/10.
1038/s41419-022-05397-1
Note: This article is intended to introduce the progress of medical research and cannot be used as a reference
for treatment options.
If you need health guidance, please go to a regular hospital
.
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