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STNM1 in human cancers: role, function and potential therapy sensitizer
Ruiqi Liu1, Xiaodong Liang1, Haiwei Guo2
1Cancer Center, Department of Radiation Oncology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, China; Graduate Department, Bengbu Medical College, Bengbu, Anhui, China.
Abstract:
STMN1 belongs to the stathmin gene family, it encodes a cytoplasmic phosphorylated protein, stathmin1, which is commonly observed in vertebrate cells. STMN1 is a structural microtubule-associated protein (MAP) that binds to microtubule protein dimers rather than microtubules, with each STMN1 binding two microtubule protein dimers and preventing their aggregation, leading to microtubule instability. STMN1 expression is elevated in a number of malignancies, and inhibition of its expression can interfere with tumor cell division. Its expression can change the division of tumor cells, thereby arresting cell growth in the G2/M phase. Moreover, STMN1 expression affects tumor cell sensitivity to anti-microtubule drug analogs, including vincristine and paclitaxel. The research on MAPs is limited, and new insights on the mechanism of STMN1 in different cancers are emerging. The effective application of STMN1 in cancer prognosis and treatment requires further understanding of this protein. Here, we summarize the general characteristics of STMN1 and outline how STMN1 plays a role in cancer development, targeting multiple signaling networks and acting as a downstream target for multiple microRNAs, circRNAs, and lincRNAs. We also summarize recent findings on the function role of STMN1 in tumor resistance and as a therapeutic target for cancer.
Insights
Stathmin (STMN1) is a microtubule-associated protein crucial for cell division. Elevated STMN1 expression in cancers impacts tumor growth, drug sensitivity, and offers potential therapeutic targets.
Area of Science:
- Molecular Biology
- Cancer Research
- Cell Biology
Background:
- Stathmin (STMN1) is a key microtubule-associated protein (MAP) regulating microtubule dynamics.
- STMN1 expression is frequently upregulated in various human malignancies.
- Understanding STMN1's role is critical for advancing cancer therapy.
Purpose of the Study:
- To summarize the characteristics of STMN1.
- To elucidate STMN1's mechanisms in cancer development and progression.
- To review STMN1's role in tumor resistance and its potential as a therapeutic target.
Main Methods:
- Literature review and synthesis of existing research on STMN1.
- Analysis of STMN1's interactions with signaling networks.
- Examination of STMN1's regulation by non-coding RNAs (microRNAs, circRNAs, lincRNAs).
Main Results:
- STMN1 destabilizes microtubules, influencing cell cycle arrest at the G2/M phase.
- STMN1 expression affects tumor cell sensitivity to anti-microtubule chemotherapy agents.
- STMN1 is implicated in multiple cancer signaling pathways and is regulated by various ncRNAs.
Conclusions:
- STMN1 is a significant factor in cancer development, progression, and therapeutic resistance.
- Targeting STMN1 holds promise for novel cancer treatment strategies.
- Further research into STMN1 mechanisms is essential for effective clinical application.
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