HMGB1’in Kanser ve Tedavisiyle İlişkisi
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Tarih
2019
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Yüksek mobilite grup kutusu 1 (HMGB1) histon olmayan DNA proteini olup, kısaca DAMP olarak ifade edilen(Damage-associated molecular pattern) tehlike sinyali veya alarmı olarak görev yapar. Hasarlanmış veya kanserlihücrelerden salınan HMGB1, gelişmiş glikasyon son ürünleri için reseptör (RAGE) ve Toll benzeri reseptörlerine(TLRs) bağlanarak mitojenle aktive olan kinaz (MAPK)’ları aktive ederek hücre içi etkilerini oluşturur. HMGB1kanser ilaçlarına karşı gelişen dirençte önemli rol oynar. Aynı zamanda, yumuşak doku kanserlerine karşıkullanılan ilaçlardan biri olan adriyamisinin (ADR) neden olduğu kalp yetmezliğinin gelişiminde de önemli roloynağına dair kanıtlar mevcuttur. Dolayısıyla HMGB1 kanser tedavisinde ilaçlara karşı gelişen direncin ve/veyailacın toksik etkisine karşı iyi bir terapötik ajan adayıdır. Bu derlemenin amacı, HMGB1 ile kanser ve tedavisindekullanılan bir ilaç olan ADR arasındaki ilişkiyi açıklamaktır.
High mobility group box-1 (HMGB1), one of nonhiston protein, plays role as danger signals, and alarming shortly named as DAMP. HMGB1 released from damaged and cancer cells triggers mitogen activated kinases (MAPK) to act intracellular effect by binding the receptor for advanced glycation end products (RAGE) and toll like receptor (TLR). HMGB1 is essential to develop resistant against anticancer drugs. In addition, there is evidence that HMGB1 participate in developing to heart failure-induced by Adriamycin, one of anticancer drug against for solid cancer. Therefore, HMGB1 could be a good candidate for drug-resistant against to cancer and/or anticancer drug toxicity. The aim of the present review is to explain the relationship between HMBG1, cancer and Adriamycin used for cancer’s treatment
High mobility group box-1 (HMGB1), one of nonhiston protein, plays role as danger signals, and alarming shortly named as DAMP. HMGB1 released from damaged and cancer cells triggers mitogen activated kinases (MAPK) to act intracellular effect by binding the receptor for advanced glycation end products (RAGE) and toll like receptor (TLR). HMGB1 is essential to develop resistant against anticancer drugs. In addition, there is evidence that HMGB1 participate in developing to heart failure-induced by Adriamycin, one of anticancer drug against for solid cancer. Therefore, HMGB1 could be a good candidate for drug-resistant against to cancer and/or anticancer drug toxicity. The aim of the present review is to explain the relationship between HMBG1, cancer and Adriamycin used for cancer’s treatment
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Kaynak
Düzce Üniversitesi Bilim ve Teknoloji Dergisi
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Cilt
7
Sayı
3
