Evaluation of Nanaoparticle Delivery System for 5- Fluorouracil and Curcumin on Squamous Cell Carcinoma Cell Line
Shaimaa Mustafa Masloub Ali;
Abstract
The prognosis for patients with head and neck squamous cell carcinoma
is determined by the stage at presentation, the extent of the tumor (Jemal
et al., 2007). Treatment of HNSCC requires a delicate balance between
complete eradication of cancer and preservation of the underlying
anatomical form and function. Thus, there are many challenges unique to
the treatment of patients with HNSCC (Prince et al., 2010).
Chemotherapeutic agents are the mainstay of treatment and include
standard cytotoxic agents alone or in combination, as well as novel
targeted biological agents (Colevas, 2006). Although chemotherapy is of
major palliative benefit in patients with symptomatic metastatic or
incurable recurrent disease, impact on survival remains unclear. The
average survival for patients receiving chemotherapy is six to eight
months, which is only slightly more compared to supportive care alone
(Goon et al., 2009). There are also several limitations for the
chemotherapeutic drugs including their bioavailability, metabolism and
toxic side effects. So due to the limitations of chemotherapeutic drugs
and the considerable toxicity associated with the cytotoxic therapies used
in HNSCC patients, the need for treatment options that improve the
clinical outcome and have less toxicity profile is pressing (Schilsky ,
2010).
143
Antimetabolite drugs, branch of anticancer drugs, work by inhibiting
essential biosynthetic processes, or by being incorporated into
macromolecules, such as DNA and RNA, and inhibiting their normal
function. The fluoropyrimidine 5-fluorouracil (5-FU) does both (Longley
et al., 2003). Curcumin has been studied in multiple human carcinomas.
The mechanisms by which curcumin exerts its anti-cancer effects are
comprehensive and diverse, targeting many levels of regulation in the
processes of cellular growth and apoptosis (Wilken et al., 2011).
is determined by the stage at presentation, the extent of the tumor (Jemal
et al., 2007). Treatment of HNSCC requires a delicate balance between
complete eradication of cancer and preservation of the underlying
anatomical form and function. Thus, there are many challenges unique to
the treatment of patients with HNSCC (Prince et al., 2010).
Chemotherapeutic agents are the mainstay of treatment and include
standard cytotoxic agents alone or in combination, as well as novel
targeted biological agents (Colevas, 2006). Although chemotherapy is of
major palliative benefit in patients with symptomatic metastatic or
incurable recurrent disease, impact on survival remains unclear. The
average survival for patients receiving chemotherapy is six to eight
months, which is only slightly more compared to supportive care alone
(Goon et al., 2009). There are also several limitations for the
chemotherapeutic drugs including their bioavailability, metabolism and
toxic side effects. So due to the limitations of chemotherapeutic drugs
and the considerable toxicity associated with the cytotoxic therapies used
in HNSCC patients, the need for treatment options that improve the
clinical outcome and have less toxicity profile is pressing (Schilsky ,
2010).
143
Antimetabolite drugs, branch of anticancer drugs, work by inhibiting
essential biosynthetic processes, or by being incorporated into
macromolecules, such as DNA and RNA, and inhibiting their normal
function. The fluoropyrimidine 5-fluorouracil (5-FU) does both (Longley
et al., 2003). Curcumin has been studied in multiple human carcinomas.
The mechanisms by which curcumin exerts its anti-cancer effects are
comprehensive and diverse, targeting many levels of regulation in the
processes of cellular growth and apoptosis (Wilken et al., 2011).
Other data
| Title | Evaluation of Nanaoparticle Delivery System for 5- Fluorouracil and Curcumin on Squamous Cell Carcinoma Cell Line | Other Titles | تقييم نظام تسليم الجزيئات النانوية لل 5 فلورويوراسيل والكوركومين على خط خلايا السرطان الحرشفى | Authors | Shaimaa Mustafa Masloub Ali | Issue Date | 2015 |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| G10522.pdf | 583.63 kB | Adobe PDF | View/Open |
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