Clinical prognostic significance of xeroderma pigmentosum group C and IFN‑γ in non‑small cell lung cancer
Lung cancer is the most common cancer in the world due to its high incidence and recurrence. Genetic instability is one of the main factors leading to its occurrence, development and poor prognosis. Decreased xeroderma pigmentosum group C (XPC) expression notably enhances the stem cell properties of...
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Veröffentlicht in: | Oncology letters 2024-06, Vol.27 (6), p.259, Article 259 |
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description | Lung cancer is the most common cancer in the world due to its high incidence and recurrence. Genetic instability is one of the main factors leading to its occurrence, development and poor prognosis. Decreased xeroderma pigmentosum group C (XPC) expression notably enhances the stem cell properties of lung cancer cells and increases their proliferation and migration. Additionally, patients with lung cancer and low XPC expression had a poor prognosis. The purpose of the present study was to analyze the effect of XPC and IFN-γ on the clinical prognosis of patients with non-small cell lung cancer (NSCLC). Lung adenocarcinoma specimens were collected from a total of 140 patients with NSCLC. Additionally, from these 140 patients, 48 paracarcinoma tissue specimens were also collected, which were later used to construct tissue microarrays. The expression of XPC and IFN-γ in cancer tissues and in paraneoplastic tissues was detected using immunohistochemistry. The prognosis and overall survival of patients were determined through telephone follow-up. The results showed a positive correlation between expression of XPC and IFN-γ in NSCLC. Additionally, high expression of both markers was associated with a favorable prognosis in patients with NSCLC. The aforementioned findings suggest that the expression of XPC and IFN-γ has prognostic value in clinical practice and is expected to become a marker for clinical application. |
doi_str_mv | 10.3892/ol.2024.14392 |
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Genetic instability is one of the main factors leading to its occurrence, development and poor prognosis. Decreased xeroderma pigmentosum group C (XPC) expression notably enhances the stem cell properties of lung cancer cells and increases their proliferation and migration. Additionally, patients with lung cancer and low XPC expression had a poor prognosis. The purpose of the present study was to analyze the effect of XPC and IFN-γ on the clinical prognosis of patients with non-small cell lung cancer (NSCLC). Lung adenocarcinoma specimens were collected from a total of 140 patients with NSCLC. Additionally, from these 140 patients, 48 paracarcinoma tissue specimens were also collected, which were later used to construct tissue microarrays. The expression of XPC and IFN-γ in cancer tissues and in paraneoplastic tissues was detected using immunohistochemistry. The prognosis and overall survival of patients were determined through telephone follow-up. The results showed a positive correlation between expression of XPC and IFN-γ in NSCLC. Additionally, high expression of both markers was associated with a favorable prognosis in patients with NSCLC. The aforementioned findings suggest that the expression of XPC and IFN-γ has prognostic value in clinical practice and is expected to become a marker for clinical application.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2024.14392</identifier><identifier>PMID: 38646492</identifier><language>eng</language><publisher>Greece: Spandidos Publications UK Ltd</publisher><subject>Alcohol ; Antibodies ; Lung cancer ; Medical prognosis ; Metastasis ; Patients ; Semiconductors ; Survival analysis</subject><ispartof>Oncology letters, 2024-06, Vol.27 (6), p.259, Article 259</ispartof><rights>Copyright: © 2024 Wang et al.</rights><rights>Copyright Spandidos Publications UK Ltd. 2024</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c316t-2a718347c2b21d2539e3619112828eda66ac0499d4ba94cb58e1e6eda629fbfb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38646492$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yongming</creatorcontrib><creatorcontrib>Wang, Weiyu</creatorcontrib><creatorcontrib>Wang, Huaijie</creatorcontrib><creatorcontrib>Qin, Liya</creatorcontrib><creatorcontrib>Zhang, Meijia</creatorcontrib><creatorcontrib>Zhang, Yong</creatorcontrib><creatorcontrib>Wang, Yubing</creatorcontrib><creatorcontrib>Hao, Changcheng</creatorcontrib><creatorcontrib>Qu, Meihua</creatorcontrib><creatorcontrib>Wang, Gongchao</creatorcontrib><title>Clinical prognostic significance of xeroderma pigmentosum group C and IFN‑γ in non‑small cell lung cancer</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Lung cancer is the most common cancer in the world due to its high incidence and recurrence. Genetic instability is one of the main factors leading to its occurrence, development and poor prognosis. Decreased xeroderma pigmentosum group C (XPC) expression notably enhances the stem cell properties of lung cancer cells and increases their proliferation and migration. Additionally, patients with lung cancer and low XPC expression had a poor prognosis. The purpose of the present study was to analyze the effect of XPC and IFN-γ on the clinical prognosis of patients with non-small cell lung cancer (NSCLC). Lung adenocarcinoma specimens were collected from a total of 140 patients with NSCLC. Additionally, from these 140 patients, 48 paracarcinoma tissue specimens were also collected, which were later used to construct tissue microarrays. The expression of XPC and IFN-γ in cancer tissues and in paraneoplastic tissues was detected using immunohistochemistry. The prognosis and overall survival of patients were determined through telephone follow-up. The results showed a positive correlation between expression of XPC and IFN-γ in NSCLC. Additionally, high expression of both markers was associated with a favorable prognosis in patients with NSCLC. The aforementioned findings suggest that the expression of XPC and IFN-γ has prognostic value in clinical practice and is expected to become a marker for clinical application.</description><subject>Alcohol</subject><subject>Antibodies</subject><subject>Lung cancer</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Patients</subject><subject>Semiconductors</subject><subject>Survival analysis</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kE1OwzAQhS0EolXpki2yxDol_oljL1FEoVIFG1hbjuNErhI72I0EO67AWbgHh-AkpKV0FjOjmU9vNA-AS5QuCBf4xrcLnGK6QJQIfAKmKBc4QSnHp8c-pxMwj3GTjpExxDk7BxPCGWVU4ClwRWud1aqFffCN83FrNYy2cbYep04b6Gv4ZoKvTOgU7G3TGbf1cehgE_zQwwIqV8HV8vHn4_P7C1oHnXdjHzvVtlCbMbWDa-BeLFyAs1q10cwPdQZelnfPxUOyfrpfFbfrRBPEtglWOeKE5hqXGFU4I8IQhgRCmGNuKsWY0ikVoqKlElSXGTfIsN0Ci7qsSzID13-641evg4lbufFDcONJSdIswyLPKR6p5I_SwccYTC37YDsV3iVK5c5g6Vu5M1juDR75q4PqUHamOtL_dpJfGz949g</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Wang, Yongming</creator><creator>Wang, Weiyu</creator><creator>Wang, Huaijie</creator><creator>Qin, Liya</creator><creator>Zhang, Meijia</creator><creator>Zhang, Yong</creator><creator>Wang, Yubing</creator><creator>Hao, Changcheng</creator><creator>Qu, Meihua</creator><creator>Wang, Gongchao</creator><general>Spandidos Publications UK Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20240601</creationdate><title>Clinical prognostic significance of xeroderma pigmentosum group C and IFN‑γ in non‑small cell lung cancer</title><author>Wang, Yongming ; 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Genetic instability is one of the main factors leading to its occurrence, development and poor prognosis. Decreased xeroderma pigmentosum group C (XPC) expression notably enhances the stem cell properties of lung cancer cells and increases their proliferation and migration. Additionally, patients with lung cancer and low XPC expression had a poor prognosis. The purpose of the present study was to analyze the effect of XPC and IFN-γ on the clinical prognosis of patients with non-small cell lung cancer (NSCLC). Lung adenocarcinoma specimens were collected from a total of 140 patients with NSCLC. Additionally, from these 140 patients, 48 paracarcinoma tissue specimens were also collected, which were later used to construct tissue microarrays. The expression of XPC and IFN-γ in cancer tissues and in paraneoplastic tissues was detected using immunohistochemistry. The prognosis and overall survival of patients were determined through telephone follow-up. The results showed a positive correlation between expression of XPC and IFN-γ in NSCLC. Additionally, high expression of both markers was associated with a favorable prognosis in patients with NSCLC. The aforementioned findings suggest that the expression of XPC and IFN-γ has prognostic value in clinical practice and is expected to become a marker for clinical application.</abstract><cop>Greece</cop><pub>Spandidos Publications UK Ltd</pub><pmid>38646492</pmid><doi>10.3892/ol.2024.14392</doi><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Antibodies Lung cancer Medical prognosis Metastasis Patients Semiconductors Survival analysis |
title | Clinical prognostic significance of xeroderma pigmentosum group C and IFN‑γ in non‑small cell lung cancer |
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