Coordination: | DOLCET ROCA, FRANCESC XAVIER |
Academic year 2023-24 |
Subject name | CELLULAR AND MOLECULAR PATHOLOGY | ||||||||||||
Code | 101510 | ||||||||||||
Semester | 1st Q(SEMESTER) CONTINUED EVALUATION | ||||||||||||
Typology |
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Course number of credits (ECTS) | 6 | ||||||||||||
Type of activity, credits, and groups |
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Coordination | DOLCET ROCA, FRANCESC XAVIER | ||||||||||||
Department | BASIC MEDICAL SCIENCES | ||||||||||||
Important information on data processing | Consult this link for more information. | ||||||||||||
Distribution of credits | Attendance class credit 6 ECTS
Non-attendance credits 15 ECTS Theory classes 3,5 ECTS Practical classes 1,5 ECTS Seminars 1 ECTS |
Teaching staff | E-mail addresses | Credits taught by teacher | Office and hour of attention |
DOLCET ROCA, FRANCESC XAVIER | xavi.dolcet@udl.cat | 9,2 | |
TARRAGONA FORADADA, JORDI | jordi.tarragona@udl.cat | ,3 |
Competence 27
Aims
To understand and know how to apply the concepts specified in the theoretical program established in the topics of the program Understand the terminology and basic scientific language related to injury, repair and cell death. Understand the most common cellular and subcellular disorders Know how to use the concepts related to these thematic contents to interpret physiological aspects and human pathology.
Competence 28
Aims
To understand and know how to apply the concepts specified in the theoretical program established in the program topics and in scheduled seminars. Understand the terminology and basic scientific language related to research and research in a molecular diagnostic laboratory. Know how to use the concepts related to these thematic contents to interpret physiological aspects and human pathology.
Competence 40
Aims
To understand and know how to apply the concepts specified in the theoretical program established in the program topics and in scheduled seminars. To know the models and systems of study in molecular and cellular pathology. Learn the basic techniques in molecular pathology through scheduled laboratory practices To know the terminology and basic scientific language related to diagnostic research in a molecular pathology laboratory.
Competence 41
Aims
To understand the main molecular diagnostic tests in a laboratory of pathological anatomy and molecular genetics Acquire practical skills in sample handling and processing. Become familiar with the basic scientific language related to research and diagnosis in a pathological anatomy laboratory.
Competence 42.
Aims
To know and apply the basic techniques of sample processing in a molecular pathology laboratory. Acquire practical skills in sample handling and processing. To know the terminology and basic scientific language related to research and research in a molecular diagnostic laboratory.
27. To nderstand and know how to recognize tissue characteristics at the cellular and molecular levels in the different situations of injury, adaptation and cell death.
28. To understand and know how to use biochemical, cytogenetic and molecular biology markers applied to clinical diagnosis.
40. To understand the methods of diagnosis and study of genetic variation
41. To know how to obtain and process a biological sample for its study by means of the different diagnostic procedures
42. To understand and understand the most common parameters used in the description of the main diagnostic tests in the laboratory
THEORY PROGRAM
CAUSES AND MECHANISMS OF PATHOGENESIS: CELL INJURY, ADAPTATION AND CELL DEATH.
1. Introduction to molecular and cellular pathology.
1.1. The branches of pathology and their relationship with other disciplines.
1.2. Contributions of molecular pathology to the knowledge of the disease.
1.3. Brief historical analysis and evolution of the Pathology.
2. Genetic and epigenetic alterations in the development of pathologies.
2.1. Genetic alterations: mutations.
2.2. Epigenetic alterations: methylation, acetylation, microRNAs and lncRNAs. 2.3. Techniques for detecting genetic and epigenetic alterations: PCR and FISH, sequencing techniques, other molecular alteration detection techniques.
2.5 Techniques for detecting protein alterations: immunohistochemistry and cytometry.
2.6. Models of study of genetic diseases.
3. Alterations in cellular communication in the development of pathologies. .
3.1. Basic mechanisms of intracellular signaling.
3.2. Alterations in reception and signal transduction as the basis of pathologies
3.3. Classification and alterations in the main signaling pathways. Examples
4. Cellular injury: causes and mechanisms.
4.1. Loss of cell homeostasis: from stress to cell injury.
4.2. Type of agents causing injury. Molecular mechanisms of cell injury.
4.3. Examples of types of injury.
5. Responses to cellular stress: cell adaptation.
5.1. Maintenance mechanisms of cell homeostasis.
5.2. Cellular adaptations of growth and differentiation: Atrophy, hypertrophy, hyperplasia, metaplasia.
5.3. Autophagy
6. Responses to cell injury: Subcellular disorders.
6.1. Water accumulation.
6.2. Intracellular deposits of triglycerides and cholesterol.
6.3. Protein deposits. Response to the accumulation of misfolded proteins (UPR).
6.4. Pigment accumulations.
6.5. Metabolic disorders of iron and copper: hemochromatosis and Wilson's disease.
6.6.Intercellular deposits of carbohydrates.
6.7.Dystrophic and metabolic calcifications.
7. Responses to irreversible cell injury: cell death.
7.1. Types and classification of cell death.
7.2 Types of necrosis.
7.3. Types, causes, morphological and molecular changes of apoptosis. Alterations of apoptosis in the development of pathologies.
7.4 Necroptosis
7.5 Other types of cell death
REACTION, RESOLUTION AND CONSEQUENCES OF THE INJURY.
8. Reaction to injury: Inflammation.
8.1. Concept and type of inflammation.
8.2 Acute inflammation
8.3.Chronic inflammation.
8.4. Chemical mediators of inflammation. Etiological agents of chronic inflammation.
8.5 Inflammation and repair mechanisms.
8.6. Inflammation in the development of diseases
9. Recovery of cell injury: repair and cell regeneration.
9.1. Cell repair and regeneration concepts.
9.2 Stem cells in cell regeneration.
9.3. Tissue repair due to scarring and fibrosis.
9.4. Stem cells in regenerative medicine.
10. Consequences of the accumulation of lesions: cell aging. 10.1.Definition of aging and senescence
10.2.Causes, characteristics and molecular mechanisms of cell aging.
11. Consequences of the accumulation of lesions: oncological pathologies.
11.1.Neoplasms: definitions and terminology. Epidemiology of cancer.
11.2 Molecular bases of cancer.
11.3.Biology of tumor growth.
DIANÒSTIC PATHOLOGY.
12. Morphological diagnosis of pathologies: I. Cytological studies. II. Biopsies
LABORATORY PRACTICES
1. Microscopic observation of samples with cell pathologies: proliferation, differentiation and cell death, cell adaptations, subcellular alterations, inflammation.
2. Determination of molecular alterations by PCR
3. Immunohistochemistry and Immunofluorescence of biomarkers. Determination of tumor invasion by immunohistochemistry
SEMINARS
Problem solving seminars based on the concepts taught in the theoretical classes.
The final grade will be the sum of the different aspects evaluated:
The maximun final mark of this subject will be 10 point. 7 points corresponding to theory (70%), 1.5 points corresponding to practical activities (15%) and 1.5 points (15%) corresponding to semminars.
Theory concepts knowledge will be evaluated by means of two tests exams. The result obtained in this exam will constitute 70% of the final mark (35% of the final mark each exam). Final theory mark will be the averaged between the two exams. THESE TWO EXAMS MUST BE PASSED INDIVIDUALY BY A MARK ABOVE 4 OUT OF 10. MARKS BELLOW 4 IN ANY OF THE TWO EXAMS WILL BE CONSIDERED AS FAIL AND WILL NOT BE AVERAGED. IN THIS CASE THE STUDENT MUST PASS A SECOND-CHANCE REMEDIAL EXAM CORRESPONDING TO THE FAILED EXAM.
Practical activities will be evaluated by a test exam accounting for 15 % of the final mark. Attendance is mandatory. NO REMEDIAL EXAM. The mark (1.5 out of 10 point) achieved in this part will be added to the theory mark.
Semminars will be evaluated by a test exam accounting for 15 % of the final mark. Attendance is mandatory. NO REMEDIAL EXAM. The mark (1.5 out of 10 point) achieved in this part will be added to the theory mark.
Rubin’s Pathology. Clinicopathologic foundations of Medicina. 7th Edition. Ed Wolters Kluwer, 2015
Robins and Cotran. Pathologic Basis of Disease. 9th Edition. Ed Elsevier Saunder, 2015.
Coleman and Tsongalis. (2010) -Essential concepts in molecular pathology. Elsevier Academic press corp.
Tubbs and Stoler. (2009). Cellular and Tissue Based Molecular Pathology. Elsevier
Cagle et al. (2009) - Basic Concepts of Molecular Pathology. Springer.