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{{WBRQuestion
{{WBRQuestion
|QuestionAuthor={{Rim}}
|QuestionAuthor={{Rim}} (Reviewed by Will Gibson)
|ExamType=USMLE Step 1
|ExamType=USMLE Step 1
|MainCategory=Immunology
|MainCategory=Immunology
Line 8: Line 8:
|MainCategory=Immunology
|MainCategory=Immunology
|SubCategory=Gastrointestinal, General Principles
|SubCategory=Gastrointestinal, General Principles
|MainCategory=Immunology
|MainCategory=Immunology
|MainCategory=Immunology
|MainCategory=Immunology
|MainCategory=Immunology
Line 20: Line 21:
|MainCategory=Immunology
|MainCategory=Immunology
|SubCategory=Gastrointestinal, General Principles
|SubCategory=Gastrointestinal, General Principles
|Prompt=A 57 year old Japanese man presents to the physician's office for abdominal fullness, weight loss, and excessive belching. Following appropriate work-up, he is diagnosed with advanced gastric cancer. Several months later, he returns to the office appearing pale and asthenic and has dyspnea and weakness on minimal exertion. On physical examination, he has skeletal muscle atrophy and fat loss. Which of the following components most likely mediates the patient's condition?
|Prompt=A 57-year-old Japanese man presents to the physician's office for abdominal fullness, weight loss, and excessive belching. Following appropriate work-up, he is diagnosed with advanced gastric cancer.  The patient undergoes treatment with 5-fluorouracil and leucovorin rescue, but his tumor failed to show an objective response and therapy is discontinued. Several months later, he returns to the office appearing pale and asthenic. He suffers from dyspnea and weakness on minimal exertion. On physical examination, he has marked skeletal muscle atrophy and fat loss. Which of the following components most likely mediates the patient's condition?
|Explanation=The patient presents with signs and symptoms consistent with cachexia, a syndrome that is characterized by the presence of anorexia, fat and skeletal muscle wasting, severe asthenia, and fatigue. Patients usually are extremely fatigued and have dyspnea and weakness on minimal exertion or even at rest. Cachexia usually is present in advanced chronic diseases, such as cancers, AIDS, tuberculosis, and other immunodeficiencies. In cancer patients, especially GI, lung, and prostate cancers, the presence of cancerous cells leads to chronic inflammation and activation of pro-inflammatory components, mainly tumor necrosis factor-alpha (TNF-alpha) which is also known as cachectin due to its major role in the syndrome, interferon-gamma (INF-gamma), and interleukin (IL)-1beta, and 6. The administration of antibodies against some of these components may sometimes help relieve the symptoms of cachexia.
|Explanation=The patient presents with signs and symptoms consistent with cachexia, a syndrome that is characterized by the presence of anorexia, fat and skeletal muscle wasting, severe asthenia, and fatigue. Patients usually are extremely fatigued and have dyspnea and weakness on minimal exertion or even at rest. Cachexia usually is present in advanced chronic diseases, such as cancers, AIDS, tuberculosis, and other immunodeficiencies. In cancer patients, the presence of cancerous cells leads to chronic inflammation and activation of pro-inflammatory components, mainly tumor necrosis factor-alpha (TNF-alpha) which is also known as cachectin due to its major role in the syndrome, interferon-gamma (INF-gamma), and interleukin (IL)-1beta, and 6. The administration of antibodies against some of these components may sometimes help relieve the symptoms of cachexia.
 
Educational Objective:
TNF-alpha (cachectin) is the main mediator of cachexia.


Reference:
Gordon JN, Green SR, Goggin PM. Cancer cachexia. Q J Med. 2005; 98:779-788.
|AnswerA=Interleukin-2 (IL-2)
|AnswerA=Interleukin-2 (IL-2)
|AnswerAExp=IL-2 is not a main mediator of cachexia syndrome.
|AnswerAExp=IL-2 is not a main mediator of cachexia syndrome. IL-2 is secreted by T cells and helps to activate other T cells.
|AnswerB=Tumor growth factor - beta (TGF-beta)
|AnswerB=Tumor growth factor - beta (TGF-beta)
|AnswerBExp=TGF-beta is not a main mediator of cachexia syndrome.
|AnswerBExp=TGF-beta is not a main mediator of cachexia syndrome.  TGF-beta is a cytokine whose physiologic functions are varied and complex. Generally, TGF-beta is thought to reduce inflammation by inhibiting cell proliferation.  
|AnswerC=IL-4
|AnswerC=IL-4
|AnswerCExp=IL-4 is not a main mediator of cachexia syndrome.
|AnswerCExp=IL-4 is not a main mediator of cachexia syndrome. IL-4 normally functions to induce the differentiation of naive T-helper cells in lymph nodes.
|AnswerD=Tumor necrosis factor - alpha (TNF-alpha)
|AnswerD=Tumor necrosis factor - alpha (TNF-alpha)
|AnswerDExp=TNF-alpha is also known as cachectin because it is the main mediator of the syndrome of cachexia.
|AnswerDExp=TNF-alpha is also known as cachectin because it is the main mediator of the syndrome of cachexia.
|AnswerE=Interferon-alpha (INF-alpha)
|AnswerE=Interferon-alpha (INF-alpha)
|AnswerEExp=INF-alpha is not a main mediator of cachexia syndrome. Nonetheless, IFN-gamma is frequently activated in cachexia.
|AnswerEExp=INF-alpha is not a main mediator of cachexia syndrome. Nonetheless, IFN-gamma is frequently activated in cachexia. IFN-gamma is normally secreted by CD4+ Th1 cells and serves to activate nearby macrophages in the presence of a viral infection. The interferons as a family have direct antiviral activity and help to induce the expression of MHC-class II in virally infected cells.
|EducationalObjectives=TNF-alpha (cachectin) is the main mediator of cachexia.
|References=Gordon JN, Green SR, Goggin PM. Cancer cachexia. Q J Med. 2005; 98:779-788.<br>
Fearon, Kenneth CH, David J. Glass, and Denis C. Guttridge. "Cancer cachexia: mediators, signaling, and metabolic pathways." Cell metabolism 16.2 (2012): 153-166. <br>
First Aid 2014 page 231
|RightAnswer=D
|RightAnswer=D
|WBRKeyword=TNF-alpha, TNF, alpha, cachexia, cachectin, anorexia, asthenia, fatigue, weakness, dyspnea, cancer, gastric, tumor, necrosis, factor, mediator, mediates, mediate
|WBRKeyword=TNF-alpha, TNF, Alpha, Cachexia, Cachectin, Anorexia, Asthenia, Fatigue, Weakness, Dyspnea, Cancer, Gastric, Tumor, Tumor necrosis factor
|Approved=No
|Approved=No
}}
}}

Revision as of 01:04, 31 December 2014

 
Author [[PageAuthor::Rim Halaby, M.D. [1] (Reviewed by Will Gibson)]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Immunology
Sub Category SubCategory::Gastrointestinal, SubCategory::General Principles
Prompt [[Prompt::A 57-year-old Japanese man presents to the physician's office for abdominal fullness, weight loss, and excessive belching. Following appropriate work-up, he is diagnosed with advanced gastric cancer. The patient undergoes treatment with 5-fluorouracil and leucovorin rescue, but his tumor failed to show an objective response and therapy is discontinued. Several months later, he returns to the office appearing pale and asthenic. He suffers from dyspnea and weakness on minimal exertion. On physical examination, he has marked skeletal muscle atrophy and fat loss. Which of the following components most likely mediates the patient's condition?]]
Answer A AnswerA::Interleukin-2 (IL-2)
Answer A Explanation AnswerAExp::IL-2 is not a main mediator of cachexia syndrome. IL-2 is secreted by T cells and helps to activate other T cells.
Answer B AnswerB::Tumor growth factor - beta (TGF-beta)
Answer B Explanation AnswerBExp::TGF-beta is not a main mediator of cachexia syndrome. TGF-beta is a cytokine whose physiologic functions are varied and complex. Generally, TGF-beta is thought to reduce inflammation by inhibiting cell proliferation.
Answer C AnswerC::IL-4
Answer C Explanation AnswerCExp::IL-4 is not a main mediator of cachexia syndrome. IL-4 normally functions to induce the differentiation of naive T-helper cells in lymph nodes.
Answer D AnswerD::Tumor necrosis factor - alpha (TNF-alpha)
Answer D Explanation AnswerDExp::TNF-alpha is also known as cachectin because it is the main mediator of the syndrome of cachexia.
Answer E AnswerE::Interferon-alpha (INF-alpha)
Answer E Explanation [[AnswerEExp::INF-alpha is not a main mediator of cachexia syndrome. Nonetheless, IFN-gamma is frequently activated in cachexia. IFN-gamma is normally secreted by CD4+ Th1 cells and serves to activate nearby macrophages in the presence of a viral infection. The interferons as a family have direct antiviral activity and help to induce the expression of MHC-class II in virally infected cells.]]
Right Answer RightAnswer::D
Explanation [[Explanation::The patient presents with signs and symptoms consistent with cachexia, a syndrome that is characterized by the presence of anorexia, fat and skeletal muscle wasting, severe asthenia, and fatigue. Patients usually are extremely fatigued and have dyspnea and weakness on minimal exertion or even at rest. Cachexia usually is present in advanced chronic diseases, such as cancers, AIDS, tuberculosis, and other immunodeficiencies. In cancer patients, the presence of cancerous cells leads to chronic inflammation and activation of pro-inflammatory components, mainly tumor necrosis factor-alpha (TNF-alpha) which is also known as cachectin due to its major role in the syndrome, interferon-gamma (INF-gamma), and interleukin (IL)-1beta, and 6. The administration of antibodies against some of these components may sometimes help relieve the symptoms of cachexia.

Educational Objective: TNF-alpha (cachectin) is the main mediator of cachexia.
References: Gordon JN, Green SR, Goggin PM. Cancer cachexia. Q J Med. 2005; 98:779-788.
Fearon, Kenneth CH, David J. Glass, and Denis C. Guttridge. "Cancer cachexia: mediators, signaling, and metabolic pathways." Cell metabolism 16.2 (2012): 153-166.
First Aid 2014 page 231]]

Approved Approved::No
Keyword WBRKeyword::TNF-alpha, WBRKeyword::TNF, WBRKeyword::Alpha, WBRKeyword::Cachexia, WBRKeyword::Cachectin, WBRKeyword::Anorexia, WBRKeyword::Asthenia, WBRKeyword::Fatigue, WBRKeyword::Weakness, WBRKeyword::Dyspnea, WBRKeyword::Cancer, WBRKeyword::Gastric, WBRKeyword::Tumor, WBRKeyword::Tumor necrosis factor
Linked Question Linked::
Order in Linked Questions LinkedOrder::