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SALL4: An Intriguing Therapeutic Target in Cancer Treatment

Spalt-Like Transcription Factor 4 (SALL4) is a critical factor for self-renewal ability and pluripotency of stem cells. On the other hand, various reports show tight relation of SALL4 to cancer occurrence and metastasis. SALL4 exerts its effects not only by inducing gene expression but also repressi...

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Autores principales: Moein, Shiva, Tenen, Daniel G., Amabile, Giovanni, Chai, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406946/
https://www.ncbi.nlm.nih.gov/pubmed/36010677
http://dx.doi.org/10.3390/cells11162601
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author Moein, Shiva
Tenen, Daniel G.
Amabile, Giovanni
Chai, Li
author_facet Moein, Shiva
Tenen, Daniel G.
Amabile, Giovanni
Chai, Li
author_sort Moein, Shiva
collection PubMed
description Spalt-Like Transcription Factor 4 (SALL4) is a critical factor for self-renewal ability and pluripotency of stem cells. On the other hand, various reports show tight relation of SALL4 to cancer occurrence and metastasis. SALL4 exerts its effects not only by inducing gene expression but also repressing a large cluster of genes through interaction with various epigenetic modifiers. Due to high expression of SALL4 in cancer cells and its silence in almost all adult tissues, it is an ideal target for cancer therapy. However, targeting SALL4 meets various challenges. SALL4 is a transcription factor and designing appropriate drug to inhibit this intra-nucleus component is challenging. On the other hand, due to lack of our knowledge on structure of the protein and the suitable active sites, it becomes more difficult to reach the appropriate drugs against SALL4. In this review, we have focused on approaches applied yet to target this oncogene and discuss the potential of degrader systems as new therapeutics to target oncogenes.
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spelling pubmed-94069462022-08-26 SALL4: An Intriguing Therapeutic Target in Cancer Treatment Moein, Shiva Tenen, Daniel G. Amabile, Giovanni Chai, Li Cells Review Spalt-Like Transcription Factor 4 (SALL4) is a critical factor for self-renewal ability and pluripotency of stem cells. On the other hand, various reports show tight relation of SALL4 to cancer occurrence and metastasis. SALL4 exerts its effects not only by inducing gene expression but also repressing a large cluster of genes through interaction with various epigenetic modifiers. Due to high expression of SALL4 in cancer cells and its silence in almost all adult tissues, it is an ideal target for cancer therapy. However, targeting SALL4 meets various challenges. SALL4 is a transcription factor and designing appropriate drug to inhibit this intra-nucleus component is challenging. On the other hand, due to lack of our knowledge on structure of the protein and the suitable active sites, it becomes more difficult to reach the appropriate drugs against SALL4. In this review, we have focused on approaches applied yet to target this oncogene and discuss the potential of degrader systems as new therapeutics to target oncogenes. MDPI 2022-08-20 /pmc/articles/PMC9406946/ /pubmed/36010677 http://dx.doi.org/10.3390/cells11162601 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Moein, Shiva
Tenen, Daniel G.
Amabile, Giovanni
Chai, Li
SALL4: An Intriguing Therapeutic Target in Cancer Treatment
title SALL4: An Intriguing Therapeutic Target in Cancer Treatment
title_full SALL4: An Intriguing Therapeutic Target in Cancer Treatment
title_fullStr SALL4: An Intriguing Therapeutic Target in Cancer Treatment
title_full_unstemmed SALL4: An Intriguing Therapeutic Target in Cancer Treatment
title_short SALL4: An Intriguing Therapeutic Target in Cancer Treatment
title_sort sall4: an intriguing therapeutic target in cancer treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406946/
https://www.ncbi.nlm.nih.gov/pubmed/36010677
http://dx.doi.org/10.3390/cells11162601
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